FAMILIAL AMYOTROPHIC-LATERAL-SCLEROSIS MOTOR-NEURON DISEASE (FALS) - A REVIEW OF CURRENT DEVELOPMENTS

被引：57

作者：

DEBELLEROCHE, J ^{[1
]}

ORRELL, R ^{[1
]}

KING, A ^{[1
]}

机构：

[1] CHARING CROSS & WESTMINSTER MED SCH,ACAD UNIT NEUROSCI,LONDON W6 8RF,ENGLAND

来源：

JOURNAL OF MEDICAL GENETICS | 1995年 / 32卷 / 11期

关键词：

D O I：

10.1136/jmg.32.11.841

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

[No abstract available]

引用

页码：841 / 847

页数：7

共 65 条

[51] MUTATIONS IN CU/ZN SUPEROXIDE-DISMUTASE GENE ARE ASSOCIATED WITH FAMILIAL AMYOTROPHIC-LATERAL-SCLEROSIS
ROSEN, DR
SIDDIQUE, T
PATTERSON, D
FIGLEWICZ, DA
SAPP, P
HENTATI, A
DONALDSON, D
GOTO, J
OREGAN, JP
DENG, HX
RAHMANI, Z
KRIZUS, A
MCKENNAYASEK, D
CAYABYAB, A
GASTON, SM
BERGER, R
TANZI, RE
HALPERIN, JJ
HERZFELDT, B
VANDENBERGH, R
HUNG, WY
BIRD, T
DENG, G
MULDER, DW
SMYTH, C
LAING, NG
SORIANO, E
PERICAKVANCE, MA
HAINES, J
ROULEAU, GA
GUSELLA, JS
HORVITZ, HR
BROWN, RH
[J]. NATURE, 1993, 362 (6415) : 59 - 62
[52] GENETIC-LINKAGE ANALYSIS OF FAMILIAL AMYOTROPHIC-LATERAL-SCLEROSIS USING HUMAN-CHROMOSOME-21 MICROSATELLITE DNA MARKERS
ROSEN, DR
SAPP, P
OREGAN, J
MCKENNAYASEK, D
SCHLUMPF, KS
HAINES, JL
GUSELLA, JF
HORVITZ, HR
BROWN, RH
[J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1994, 51 (01): : 61 - 69
[53] SENTNER M, 1992, NATURE, V358, P502
[54] SENTNER M, 1990, NATURE, V345, P440
[55] LINKAGE OF A GENE CAUSING FAMILIAL AMYOTROPHIC-LATERAL-SCLEROSIS TO CHROMOSOME-21 AND EVIDENCE OF GENETIC-LOCUS HETEROGENEITY
SIDDIQUE, T
FIGLEWICZ, DA
PERICAKVANCE, MA
HAINES, JL
ROULEAU, G
JEFFERS, AJ
SAPP, P
HUNG, WY
BEBOUT, J
MCKENNAYASEK, D
DENG, G
HORVITZ, HR
GUSELLA, JF
BROWN, RH
ROSES, AD
[J]. NEW ENGLAND JOURNAL OF MEDICINE, 1991, 324 (20) : 1381 - 1384
[56] Siddique T., 1994, American Journal of Human Genetics, V55, pA243
[57] X-LINKED RECESSIVE BULBOSPINAL NEURONOPATHY - A CLINICOPATHOLOGICAL STUDY
SOBUE, G
HASHIZUME, Y
MUKAI, E
HIRAYAMA, M
MITSUMA, T
TAKAHASHI, A
[J]. BRAIN, 1989, 112 : 209 - 232
[58] FAMILIAL AMYOTROPHIC-LATERAL-SCLEROSIS, 1850-1989 - A STATISTICAL-ANALYSIS OF THE WORLD LITERATURE
STRONG, MJ
HUDSON, AJ
ALVORD, WG
[J]. CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES, 1991, 18 (01) : 45 - 58
[59] A NULL MUTATION IN THE HUMAN CNTF GENE IS NOT CAUSALLY RELATED TO NEUROLOGICAL DISEASES
TAKAHASHI, R
YOKOJI, H
MISAWA, H
HAYASHI, M
HU, JG
DEGUCHI, T
[J]. NATURE GENETICS, 1994, 7 (01) : 79 - 84
[60] ANALYSIS OF THE FUNCTIONAL-EFFECTS OF A MUTATION IN SOD1 ASSOCIATED WITH FAMILIAL AMYOTROPHIC-LATERAL-SCLEROSIS
TSUDA, T
MUNTHASSER, S
FRASER, PE
PERCY, ME
RAINERO, I
VAULA, G
PINESSI, L
BERGAMINI, L
VIGNOCCHI, G
MCLACHLAN, DRC
TATTON, WG
SAINTGEORGEHYSLOP, P
[J]. NEURON, 1994, 13 (03) : 727 - 736

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