共 4 条
[1]
Mutations in PCSK9 cause autosomal dominant hypercholesterolemia
[J].
Abifadel, M
;
Varret, M
;
Rabès, JP
;
Allard, D
;
Ouguerram, K
;
Devillers, M
;
Cruaud, C
;
Benjannet, S
;
Wickham, L
;
Erlich, D
;
Derré, A
;
Villéger, L
;
Farnier, M
;
Beucler, I
;
Bruckert, E
;
Chambaz, J
;
Chanu, B
;
Lecerf, JM
;
Luc, G
;
Moulin, P
;
Weissenbach, J
;
Prat, A
;
Krempf, M
;
Junien, C
;
Seidah, NG
;
Boileau, C
.
NATURE GENETICS,
2003, 34 (02)
:154-156

Abifadel, M
论文数: 0 引用数: 0
h-index: 0
机构: Univ Paris 05, INSERM, U383, Hop Necker Enfants Malad,APHP, F-75743 Paris 15, France

Varret, M
论文数: 0 引用数: 0
h-index: 0
机构: Univ Paris 05, INSERM, U383, Hop Necker Enfants Malad,APHP, F-75743 Paris 15, France

Rabès, JP
论文数: 0 引用数: 0
h-index: 0
机构: Univ Paris 05, INSERM, U383, Hop Necker Enfants Malad,APHP, F-75743 Paris 15, France

Allard, D
论文数: 0 引用数: 0
h-index: 0
机构: Univ Paris 05, INSERM, U383, Hop Necker Enfants Malad,APHP, F-75743 Paris 15, France

Ouguerram, K
论文数: 0 引用数: 0
h-index: 0
机构: Univ Paris 05, INSERM, U383, Hop Necker Enfants Malad,APHP, F-75743 Paris 15, France

Devillers, M
论文数: 0 引用数: 0
h-index: 0
机构: Univ Paris 05, INSERM, U383, Hop Necker Enfants Malad,APHP, F-75743 Paris 15, France

Cruaud, C
论文数: 0 引用数: 0
h-index: 0
机构: Univ Paris 05, INSERM, U383, Hop Necker Enfants Malad,APHP, F-75743 Paris 15, France

Benjannet, S
论文数: 0 引用数: 0
h-index: 0
机构: Univ Paris 05, INSERM, U383, Hop Necker Enfants Malad,APHP, F-75743 Paris 15, France

Wickham, L
论文数: 0 引用数: 0
h-index: 0
机构: Univ Paris 05, INSERM, U383, Hop Necker Enfants Malad,APHP, F-75743 Paris 15, France

Erlich, D
论文数: 0 引用数: 0
h-index: 0
机构: Univ Paris 05, INSERM, U383, Hop Necker Enfants Malad,APHP, F-75743 Paris 15, France

Derré, A
论文数: 0 引用数: 0
h-index: 0
机构: Univ Paris 05, INSERM, U383, Hop Necker Enfants Malad,APHP, F-75743 Paris 15, France

Villéger, L
论文数: 0 引用数: 0
h-index: 0
机构: Univ Paris 05, INSERM, U383, Hop Necker Enfants Malad,APHP, F-75743 Paris 15, France

Farnier, M
论文数: 0 引用数: 0
h-index: 0
机构: Univ Paris 05, INSERM, U383, Hop Necker Enfants Malad,APHP, F-75743 Paris 15, France

Beucler, I
论文数: 0 引用数: 0
h-index: 0
机构: Univ Paris 05, INSERM, U383, Hop Necker Enfants Malad,APHP, F-75743 Paris 15, France

Bruckert, E
论文数: 0 引用数: 0
h-index: 0
机构: Univ Paris 05, INSERM, U383, Hop Necker Enfants Malad,APHP, F-75743 Paris 15, France

Chambaz, J
论文数: 0 引用数: 0
h-index: 0
机构: Univ Paris 05, INSERM, U383, Hop Necker Enfants Malad,APHP, F-75743 Paris 15, France

Chanu, B
论文数: 0 引用数: 0
h-index: 0
机构: Univ Paris 05, INSERM, U383, Hop Necker Enfants Malad,APHP, F-75743 Paris 15, France

Lecerf, JM
论文数: 0 引用数: 0
h-index: 0
机构: Univ Paris 05, INSERM, U383, Hop Necker Enfants Malad,APHP, F-75743 Paris 15, France

Luc, G
论文数: 0 引用数: 0
h-index: 0
机构: Univ Paris 05, INSERM, U383, Hop Necker Enfants Malad,APHP, F-75743 Paris 15, France

Moulin, P
论文数: 0 引用数: 0
h-index: 0
机构: Univ Paris 05, INSERM, U383, Hop Necker Enfants Malad,APHP, F-75743 Paris 15, France

Weissenbach, J
论文数: 0 引用数: 0
h-index: 0
机构: Univ Paris 05, INSERM, U383, Hop Necker Enfants Malad,APHP, F-75743 Paris 15, France

Prat, A
论文数: 0 引用数: 0
h-index: 0
机构: Univ Paris 05, INSERM, U383, Hop Necker Enfants Malad,APHP, F-75743 Paris 15, France

Krempf, M
论文数: 0 引用数: 0
h-index: 0
机构: Univ Paris 05, INSERM, U383, Hop Necker Enfants Malad,APHP, F-75743 Paris 15, France

Junien, C
论文数: 0 引用数: 0
h-index: 0
机构: Univ Paris 05, INSERM, U383, Hop Necker Enfants Malad,APHP, F-75743 Paris 15, France

Seidah, NG
论文数: 0 引用数: 0
h-index: 0
机构: Univ Paris 05, INSERM, U383, Hop Necker Enfants Malad,APHP, F-75743 Paris 15, France

Boileau, C
论文数: 0 引用数: 0
h-index: 0
机构: Univ Paris 05, INSERM, U383, Hop Necker Enfants Malad,APHP, F-75743 Paris 15, France
[2]
ABIFADEL M, 2005, HUM MUTAT
[3]
LOVD: Easy creation of a locus-specific sequence variation database using an "LSDB-in-a-Box" approach
[J].
Fokkema, IFAC
;
den Dunnen, JT
;
Taschner, PEM
.
HUMAN MUTATION,
2005, 26 (02)
:63-68

Fokkema, IFAC
论文数: 0 引用数: 0
h-index: 0
机构:
Leiden Univ, Ctr Med, Ctr Human & Clin Genet, NL-2300 RA Leiden, Netherlands Leiden Univ, Ctr Med, Ctr Human & Clin Genet, NL-2300 RA Leiden, Netherlands

den Dunnen, JT
论文数: 0 引用数: 0
h-index: 0
机构:
Leiden Univ, Ctr Med, Ctr Human & Clin Genet, NL-2300 RA Leiden, Netherlands Leiden Univ, Ctr Med, Ctr Human & Clin Genet, NL-2300 RA Leiden, Netherlands

Taschner, PEM
论文数: 0 引用数: 0
h-index: 0
机构:
Leiden Univ, Ctr Med, Ctr Human & Clin Genet, NL-2300 RA Leiden, Netherlands Leiden Univ, Ctr Med, Ctr Human & Clin Genet, NL-2300 RA Leiden, Netherlands
[4]
Update and analysis of the University College London Low Density Lipoprotein receptor familial hypercholesterolemia database
[J].
Leigh, S. E. A.
;
Foster, A. H.
;
Whittall, R. A.
;
Hubbart, C. S.
;
Humphries, S. E.
.
ANNALS OF HUMAN GENETICS,
2008, 72
:485-498

Leigh, S. E. A.
论文数: 0 引用数: 0
h-index: 0
机构:
UCL Royal Free & Univ Coll Med Sch, British Heart Fdn Labs, Ctr Cardiovasc Genet, London WC1E 6JJ, England UCL Royal Free & Univ Coll Med Sch, British Heart Fdn Labs, Ctr Cardiovasc Genet, London WC1E 6JJ, England

Foster, A. H.
论文数: 0 引用数: 0
h-index: 0
机构:
UCL Royal Free & Univ Coll Med Sch, British Heart Fdn Labs, Ctr Cardiovasc Genet, London WC1E 6JJ, England UCL Royal Free & Univ Coll Med Sch, British Heart Fdn Labs, Ctr Cardiovasc Genet, London WC1E 6JJ, England

Whittall, R. A.
论文数: 0 引用数: 0
h-index: 0
机构:
UCL Royal Free & Univ Coll Med Sch, British Heart Fdn Labs, Ctr Cardiovasc Genet, London WC1E 6JJ, England UCL Royal Free & Univ Coll Med Sch, British Heart Fdn Labs, Ctr Cardiovasc Genet, London WC1E 6JJ, England

Hubbart, C. S.
论文数: 0 引用数: 0
h-index: 0
机构:
UCL Royal Free & Univ Coll Med Sch, British Heart Fdn Labs, Ctr Cardiovasc Genet, London WC1E 6JJ, England UCL Royal Free & Univ Coll Med Sch, British Heart Fdn Labs, Ctr Cardiovasc Genet, London WC1E 6JJ, England

Humphries, S. E.
论文数: 0 引用数: 0
h-index: 0
机构:
UCL Royal Free & Univ Coll Med Sch, British Heart Fdn Labs, Ctr Cardiovasc Genet, London WC1E 6JJ, England UCL Royal Free & Univ Coll Med Sch, British Heart Fdn Labs, Ctr Cardiovasc Genet, London WC1E 6JJ, England
