Expanding the spectrum of POMT1 mutations: limb-girdle muscular dystrophy with mental retardation and microcephaly (LGMD2K)

被引：0
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作者：
Cirak, Sebahattin
Uyanik, Goekhan
Herrmann, Ralf
Gross, Claudia
Hehr, Ute
Voit, Thomas
机构：
[1] Univ Childrens Hosp Essen, Essen, Germany
[2] Dept Neurol, D-8400 Regensburg, Germany
[3] Ctr Human Genet, Regensburg, Germany
来源：
NEUROMUSCULAR DISORDERS | 2006年 / 16卷
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R74 [神经病学与精神病学];
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页码：S77 / S77
页数：1
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