共 19 条
[1]
Congenital cataracts facial dysmorphism neuropathy (CCFDN) syndrome: a novel developmental disorder in Gypsies maps to 18qter
[J].
Angelicheva, D
;
Turnev, I
;
Dye, D
;
Chandler, D
;
Thomas, PK
;
Kalaydjieva, L
.
EUROPEAN JOURNAL OF HUMAN GENETICS,
1999, 7 (05)
:560-566

Angelicheva, D
论文数: 0 引用数: 0
h-index: 0
机构: Edith Cowan Univ, Ctr Human Genet, Perth, WA 6027, Australia

Turnev, I
论文数: 0 引用数: 0
h-index: 0
机构: Edith Cowan Univ, Ctr Human Genet, Perth, WA 6027, Australia

Dye, D
论文数: 0 引用数: 0
h-index: 0
机构: Edith Cowan Univ, Ctr Human Genet, Perth, WA 6027, Australia

Chandler, D
论文数: 0 引用数: 0
h-index: 0
机构: Edith Cowan Univ, Ctr Human Genet, Perth, WA 6027, Australia

Thomas, PK
论文数: 0 引用数: 0
h-index: 0
机构: Edith Cowan Univ, Ctr Human Genet, Perth, WA 6027, Australia

Kalaydjieva, L
论文数: 0 引用数: 0
h-index: 0
机构: Edith Cowan Univ, Ctr Human Genet, Perth, WA 6027, Australia
[2]
Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21
[J].
Baxter, RV
;
Ben Othmane, K
;
Rochelle, JM
;
Stajich, JE
;
Hulette, C
;
Dew-Knight, S
;
Hentati, F
;
Ben Hamida, M
;
Bel, S
;
Stenger, JE
;
Gilbert, JR
;
Pericak-Vance, MA
;
Vance, JM
.
NATURE GENETICS,
2002, 30 (01)
:21-22

Baxter, RV
论文数: 0 引用数: 0
h-index: 0
机构: Duke Univ, Med Ctr, Inst Genom Sci & Policy, Ctr Human Genet, Durham, NC 27710 USA

Ben Othmane, K
论文数: 0 引用数: 0
h-index: 0
机构: Duke Univ, Med Ctr, Inst Genom Sci & Policy, Ctr Human Genet, Durham, NC 27710 USA

Rochelle, JM
论文数: 0 引用数: 0
h-index: 0
机构: Duke Univ, Med Ctr, Inst Genom Sci & Policy, Ctr Human Genet, Durham, NC 27710 USA

Stajich, JE
论文数: 0 引用数: 0
h-index: 0
机构: Duke Univ, Med Ctr, Inst Genom Sci & Policy, Ctr Human Genet, Durham, NC 27710 USA

Hulette, C
论文数: 0 引用数: 0
h-index: 0
机构: Duke Univ, Med Ctr, Inst Genom Sci & Policy, Ctr Human Genet, Durham, NC 27710 USA

Dew-Knight, S
论文数: 0 引用数: 0
h-index: 0
机构: Duke Univ, Med Ctr, Inst Genom Sci & Policy, Ctr Human Genet, Durham, NC 27710 USA

Hentati, F
论文数: 0 引用数: 0
h-index: 0
机构: Duke Univ, Med Ctr, Inst Genom Sci & Policy, Ctr Human Genet, Durham, NC 27710 USA

Ben Hamida, M
论文数: 0 引用数: 0
h-index: 0
机构: Duke Univ, Med Ctr, Inst Genom Sci & Policy, Ctr Human Genet, Durham, NC 27710 USA

Bel, S
论文数: 0 引用数: 0
h-index: 0
机构: Duke Univ, Med Ctr, Inst Genom Sci & Policy, Ctr Human Genet, Durham, NC 27710 USA

Stenger, JE
论文数: 0 引用数: 0
h-index: 0
机构: Duke Univ, Med Ctr, Inst Genom Sci & Policy, Ctr Human Genet, Durham, NC 27710 USA

Gilbert, JR
论文数: 0 引用数: 0
h-index: 0
机构: Duke Univ, Med Ctr, Inst Genom Sci & Policy, Ctr Human Genet, Durham, NC 27710 USA

Pericak-Vance, MA
论文数: 0 引用数: 0
h-index: 0
机构: Duke Univ, Med Ctr, Inst Genom Sci & Policy, Ctr Human Genet, Durham, NC 27710 USA

Vance, JM
论文数: 0 引用数: 0
h-index: 0
机构: Duke Univ, Med Ctr, Inst Genom Sci & Policy, Ctr Human Genet, Durham, NC 27710 USA
[3]
Identification of a new locus for autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin on chromosome 11p15
[J].
Ben Othmane, K
;
Johnson, E
;
Menold, M
;
Graham, FL
;
Ben Hamida, M
;
Hasegawa, O
;
Rogala, AD
;
Ohnishi, A
;
Pericak-Vance, M
;
Hentati, F
;
Vance, JM
.
GENOMICS,
1999, 62 (03)
:344-349

Ben Othmane, K
论文数: 0 引用数: 0
h-index: 0
机构: Duke Univ, Med Ctr, Dept Med, Div Neurol, Durham, NC 27710 USA

Johnson, E
论文数: 0 引用数: 0
h-index: 0
机构: Duke Univ, Med Ctr, Dept Med, Div Neurol, Durham, NC 27710 USA

Menold, M
论文数: 0 引用数: 0
h-index: 0
机构: Duke Univ, Med Ctr, Dept Med, Div Neurol, Durham, NC 27710 USA

Graham, FL
论文数: 0 引用数: 0
h-index: 0
机构: Duke Univ, Med Ctr, Dept Med, Div Neurol, Durham, NC 27710 USA

Ben Hamida, M
论文数: 0 引用数: 0
h-index: 0
机构: Duke Univ, Med Ctr, Dept Med, Div Neurol, Durham, NC 27710 USA

Hasegawa, O
论文数: 0 引用数: 0
h-index: 0
机构: Duke Univ, Med Ctr, Dept Med, Div Neurol, Durham, NC 27710 USA

Rogala, AD
论文数: 0 引用数: 0
h-index: 0
机构: Duke Univ, Med Ctr, Dept Med, Div Neurol, Durham, NC 27710 USA

Ohnishi, A
论文数: 0 引用数: 0
h-index: 0
机构: Duke Univ, Med Ctr, Dept Med, Div Neurol, Durham, NC 27710 USA

Pericak-Vance, M
论文数: 0 引用数: 0
h-index: 0
机构: Duke Univ, Med Ctr, Dept Med, Div Neurol, Durham, NC 27710 USA

Hentati, F
论文数: 0 引用数: 0
h-index: 0
机构: Duke Univ, Med Ctr, Dept Med, Div Neurol, Durham, NC 27710 USA

Vance, JM
论文数: 0 引用数: 0
h-index: 0
机构: Duke Univ, Med Ctr, Dept Med, Div Neurol, Durham, NC 27710 USA
[4]
The physical maps for sequencing human chromosomes 1, 6, 9, 10, 13, 20 and X
[J].
Bentley, DR
;
Deloukas, P
;
Dunham, A
;
French, L
;
Gregory, SG
;
Humphray, SJ
;
Mungall, AJ
;
Ross, MT
;
Carter, NP
;
Dunham, I
;
Scott, CE
;
Ashcroft, KJ
;
Atkinson, AL
;
Aubin, K
;
Beare, DM
;
Bethel, G
;
Brady, N
;
Brook, JC
;
Burford, DC
;
Burrill, WD
;
Burrows, C
;
Butler, AP
;
Carder, C
;
Catanese, JJ
;
Clee, CM
;
Clegg, SM
;
Cobley, V
;
Coffey, AJ
;
Cole, CG
;
Collins, JE
;
Conquer, JS
;
Cooper, RA
;
Culley, KM
;
Dawson, E
;
Dearden, FL
;
Durbin, RM
;
de Jong, PJ
;
Dhami, PD
;
Earthrowl, ME
;
Edwards, CA
;
Evans, RS
;
Gillson, CJ
;
Ghori, J
;
Green, L
;
Gwilliam, R
;
Halls, KS
;
Hammond, S
;
Harper, GL
;
Heathcott, RW
;
Holden, JL
.
NATURE,
2001, 409 (6822)
:942-943

Bentley, DR
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England

Deloukas, P
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England

Dunham, A
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England

French, L
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England

Gregory, SG
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England

Humphray, SJ
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England

Mungall, AJ
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England

Ross, MT
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England

Carter, NP
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England

Dunham, I
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England

Scott, CE
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England

Ashcroft, KJ
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England

Atkinson, AL
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England

Aubin, K
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England

Beare, DM
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England

Bethel, G
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England

Brady, N
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England

Brook, JC
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England

Burford, DC
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England

Burrill, WD
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England

Burrows, C
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England

Butler, AP
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England

Carder, C
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England

Catanese, JJ
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England

Clee, CM
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England

Clegg, SM
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England

Cobley, V
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England

Coffey, AJ
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England

Cole, CG
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England

Collins, JE
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England

Conquer, JS
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England

Cooper, RA
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England

Culley, KM
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England

Dawson, E
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England

Dearden, FL
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England

Durbin, RM
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England

de Jong, PJ
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England

Dhami, PD
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England

Earthrowl, ME
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England

Edwards, CA
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England

Evans, RS
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England

Gillson, CJ
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England

Ghori, J
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England

Green, L
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England

Gwilliam, R
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England

Halls, KS
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England

Hammond, S
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England

Harper, GL
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England

Heathcott, RW
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England

Holden, JL
论文数: 0 引用数: 0
h-index: 0
机构: Sanger Ctr, Cambridge CB10 1SA, England
[5]
Periaxin mutations cause recessive Dejerine-Sottas neuropathy
[J].
Boerkoel, CF
;
Takashima, H
;
Stankiewicz, P
;
Garcia, CA
;
Leber, SM
;
Rhee-Morris, L
;
Lupski, JR
.
AMERICAN JOURNAL OF HUMAN GENETICS,
2001, 68 (02)
:325-333

Boerkoel, CF
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA

Takashima, H
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA

Stankiewicz, P
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA

Garcia, CA
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA

Leber, SM
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA

Rhee-Morris, L
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA

Lupski, JR
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
[6]
Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2
[J].
Bolino, A
;
Muglia, M
;
Conforti, FL
;
LeGuern, E
;
Salih, MAM
;
Georgiou, DM
;
Christodoulou, K
;
Hausmanowa-Petrusewicz, I
;
Mandich, P
;
Schenone, A
;
Gambardella, A
;
Bono, F
;
Quattrone, A
;
Devoto, M
;
Monaco, AP
.
NATURE GENETICS,
2000, 25 (01)
:17-19

Bolino, A
论文数: 0 引用数: 0
h-index: 0
机构: Wellcome Trust Ctr Human Genet, Oxford, England

Muglia, M
论文数: 0 引用数: 0
h-index: 0
机构: Wellcome Trust Ctr Human Genet, Oxford, England

Conforti, FL
论文数: 0 引用数: 0
h-index: 0
机构: Wellcome Trust Ctr Human Genet, Oxford, England

LeGuern, E
论文数: 0 引用数: 0
h-index: 0
机构: Wellcome Trust Ctr Human Genet, Oxford, England

Salih, MAM
论文数: 0 引用数: 0
h-index: 0
机构: Wellcome Trust Ctr Human Genet, Oxford, England

Georgiou, DM
论文数: 0 引用数: 0
h-index: 0
机构: Wellcome Trust Ctr Human Genet, Oxford, England

论文数: 引用数:
h-index:
机构:

Hausmanowa-Petrusewicz, I
论文数: 0 引用数: 0
h-index: 0
机构: Wellcome Trust Ctr Human Genet, Oxford, England

Mandich, P
论文数: 0 引用数: 0
h-index: 0
机构: Wellcome Trust Ctr Human Genet, Oxford, England

Schenone, A
论文数: 0 引用数: 0
h-index: 0
机构: Wellcome Trust Ctr Human Genet, Oxford, England

Gambardella, A
论文数: 0 引用数: 0
h-index: 0
机构: Wellcome Trust Ctr Human Genet, Oxford, England

Bono, F
论文数: 0 引用数: 0
h-index: 0
机构: Wellcome Trust Ctr Human Genet, Oxford, England

Quattrone, A
论文数: 0 引用数: 0
h-index: 0
机构: Wellcome Trust Ctr Human Genet, Oxford, England

Devoto, M
论文数: 0 引用数: 0
h-index: 0
机构: Wellcome Trust Ctr Human Genet, Oxford, England

Monaco, AP
论文数: 0 引用数: 0
h-index: 0
机构:
Wellcome Trust Ctr Human Genet, Oxford, England Wellcome Trust Ctr Human Genet, Oxford, England
[7]
Hereditary motor and sensory neuropathy Lom (HMSNL): refined genetic mapping in Romani (Gypsy) families from several European countries
[J].
Chandler, D
;
Angelicheva, D
;
Heather, L
;
Gooding, R
;
Gresham, D
;
Yanakiev, P
;
de Jonge, R
;
Baas, F
;
Dye, D
;
Karagyozov, L
;
Savov, A
;
Blechschmidt, K
;
Keats, B
;
Thomas, PK
;
King, RHM
;
Starr, A
;
Nikolova, A
;
Colomer, J
;
Ishpekova, B
;
Tournev, I
;
Urtizberea, JA
;
Merlini, L
;
Butinar, D
;
Chabrol, B
;
Voit, T
;
Baethmann, M
;
Nedkova, V
;
Corches, A
;
Kalaydjieva, L
.
NEUROMUSCULAR DISORDERS,
2000, 10 (08)
:584-591

Chandler, D
论文数: 0 引用数: 0
h-index: 0
机构: Edith Cowan Univ, Ctr Human Genet, Perth, WA 6027, Australia

Angelicheva, D
论文数: 0 引用数: 0
h-index: 0
机构: Edith Cowan Univ, Ctr Human Genet, Perth, WA 6027, Australia

Heather, L
论文数: 0 引用数: 0
h-index: 0
机构: Edith Cowan Univ, Ctr Human Genet, Perth, WA 6027, Australia

Gooding, R
论文数: 0 引用数: 0
h-index: 0
机构: Edith Cowan Univ, Ctr Human Genet, Perth, WA 6027, Australia

Gresham, D
论文数: 0 引用数: 0
h-index: 0
机构: Edith Cowan Univ, Ctr Human Genet, Perth, WA 6027, Australia

Yanakiev, P
论文数: 0 引用数: 0
h-index: 0
机构: Edith Cowan Univ, Ctr Human Genet, Perth, WA 6027, Australia

de Jonge, R
论文数: 0 引用数: 0
h-index: 0
机构: Edith Cowan Univ, Ctr Human Genet, Perth, WA 6027, Australia

Baas, F
论文数: 0 引用数: 0
h-index: 0
机构: Edith Cowan Univ, Ctr Human Genet, Perth, WA 6027, Australia

Dye, D
论文数: 0 引用数: 0
h-index: 0
机构: Edith Cowan Univ, Ctr Human Genet, Perth, WA 6027, Australia

Karagyozov, L
论文数: 0 引用数: 0
h-index: 0
机构: Edith Cowan Univ, Ctr Human Genet, Perth, WA 6027, Australia

Savov, A
论文数: 0 引用数: 0
h-index: 0
机构: Edith Cowan Univ, Ctr Human Genet, Perth, WA 6027, Australia

Blechschmidt, K
论文数: 0 引用数: 0
h-index: 0
机构: Edith Cowan Univ, Ctr Human Genet, Perth, WA 6027, Australia

Keats, B
论文数: 0 引用数: 0
h-index: 0
机构: Edith Cowan Univ, Ctr Human Genet, Perth, WA 6027, Australia

Thomas, PK
论文数: 0 引用数: 0
h-index: 0
机构: Edith Cowan Univ, Ctr Human Genet, Perth, WA 6027, Australia

King, RHM
论文数: 0 引用数: 0
h-index: 0
机构: Edith Cowan Univ, Ctr Human Genet, Perth, WA 6027, Australia

Starr, A
论文数: 0 引用数: 0
h-index: 0
机构: Edith Cowan Univ, Ctr Human Genet, Perth, WA 6027, Australia

Nikolova, A
论文数: 0 引用数: 0
h-index: 0
机构: Edith Cowan Univ, Ctr Human Genet, Perth, WA 6027, Australia

Colomer, J
论文数: 0 引用数: 0
h-index: 0
机构: Edith Cowan Univ, Ctr Human Genet, Perth, WA 6027, Australia

Ishpekova, B
论文数: 0 引用数: 0
h-index: 0
机构: Edith Cowan Univ, Ctr Human Genet, Perth, WA 6027, Australia

Tournev, I
论文数: 0 引用数: 0
h-index: 0
机构: Edith Cowan Univ, Ctr Human Genet, Perth, WA 6027, Australia

Urtizberea, JA
论文数: 0 引用数: 0
h-index: 0
机构: Edith Cowan Univ, Ctr Human Genet, Perth, WA 6027, Australia

Merlini, L
论文数: 0 引用数: 0
h-index: 0
机构: Edith Cowan Univ, Ctr Human Genet, Perth, WA 6027, Australia

Butinar, D
论文数: 0 引用数: 0
h-index: 0
机构: Edith Cowan Univ, Ctr Human Genet, Perth, WA 6027, Australia

Chabrol, B
论文数: 0 引用数: 0
h-index: 0
机构: Edith Cowan Univ, Ctr Human Genet, Perth, WA 6027, Australia

Voit, T
论文数: 0 引用数: 0
h-index: 0
机构: Edith Cowan Univ, Ctr Human Genet, Perth, WA 6027, Australia

Baethmann, M
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