Mutations in SEPN1 cause congenital muscular dystrophy with spinal rigidity and restrictive respiratory syndrome

被引:235
作者
Moghadaszadeh, B
Petit, N
Jaillard, C
Brockington, M
Roy, SQ
Merlini, L
Romero, N
Estournet, B
Desguerre, I
Chaigne, D
Muntoni, F
Topaloglu, H
Guicheney, P
机构
[1] Grp Hosp Pitie Salpetriere, Inst Myol, INSERM, U523, F-75651 Paris 13, France
[2] Hammersmith Hosp, Imperial Coll Sch Med, Dept Paediat & Neonatal Med, London, England
[3] Hop Ray Poincare, Garches, France
[4] Rizzoli Orthoped Inst, Bologna, Italy
[5] Hop St Vincent de Paul, Serv Neuropediat, F-75674 Paris, France
[6] Clin St Odile, Strasbourg, France
[7] Hacettepe Childrens Hosp Med Ctr, Dept Paediat Neurol, Ankara, Turkey
关键词
D O I
10.1038/ng713
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
One form of congenital muscular dystrophy, rigid spine syndrome (MIM 602771), is a rare neuromuscular disorder characterized by early rigidity of the spine and respiratory insufficiency. A locus on 1p35-36 (RSMD1) was recently found to segregate with rigid spine muscular dystrophy 1 (ref. 1). Here we refine the locus and find evidence of linkage disequilibrium associated with SEPN1, which encodes the recently described selenoprotein N (ref. 2). Our identification and analysis of mutations in SEPN1 is the first description of a selenoprotein implicated in a human disease.
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页码:17 / 18
页数:2
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