Autosomal recessive mutations of GPR126 are responsible for severe Arthrogryposis multiplex congenita

被引：0

作者：

Ravenscroft, G. ^{[1
]}

Nolen, F. ^{[2
]}

Rajagopalan, S. ^{[3
]}

Meireles, A. ^{[4
]}

Paavola, K. ^{[4
]}

Gaillard, D. ^{[5
]}

Alanio, E. ^{[5
]}

Buckland, M. ^{[6
]}

Arbuckle, S. ^{[7
]}

Krivanek, M. ^{[7
]}

Maluenda, J. ^{[2
]}

Pannell, S. ^{[1
]}

Gooding, R. ^{[8
]}

Ong, R. ^{[1
]}

Allcock, R. ^{[9
]}

Kok, F. ^{[10
]}

Talbot, W. ^{[11
]}

Melki, J. ^{[2
]}

Laing, N. ^{[1
]}

机构：

[1] Harry Perkins Inst Med Res, Nedlands, WA, Australia

[2] Univ Paris South, Unite Mixte Rech, Le Kremlin Bicetre, France

[3] Liverpool Hosp, Dept Clin Genet, Liverpool, NSW, Australia

[4] Stanford Univ, Dept Dev Biol, Stanford, CA 94305 USA

[5] Pol Bouin Lab, Reims, France

[6] Brain & Mind Res Inst, Sydney, NSW, Australia

[7] Childrens Hosp Westmead, Pathol, Westmead, NSW, Australia

[8] Dept Diagnost Genom, PathWest Lab Med, Nedlands, WA, Australia

[9] Univ Western Australia, Lotterywest State Biomed Facil Genom, Nedlands, WA 6009, Australia

[10] Univ Sao Paulo, Human Genome & Stem Cell Res Ctr, Biosci Inst, Sao Paulo, Brazil

[11] Stanford Univ, Dept Clin Genet, Stanford, CA 94305 USA

来源：

NEUROMUSCULAR DISORDERS | 2015年 / 25卷

关键词：

D O I：

10.1016/j.nmd.2015.06.013

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

G.O.4

引用

页码：S186 / S186

页数：1

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