A novel mutation of CLCN1(G276C) with variable phenotype of Thomsen disease in a Korean family

被引：0

作者：

Suh, G. ^{[1
]}

Hong, J. ^{[1
]}

Shim, D. ^{[2
]}

Kim, D. ^{[3
]}

Choi, Y. ^{[1
]}

机构：

[1] Yonsei Univ, Coll Med, Dept Neurol, Brain Korea Project Med Sci 21, Seoul, South Korea

[2] Catholic Univ Korea, Coll Med, Dept Neurol, Seoul, South Korea

[3] Pusan Natl Univ, Yangsan Hosp, Dept Neurol, Yangsan, South Korea

来源：

NEUROMUSCULAR DISORDERS | 2010年 / 20卷 / 9-10期

关键词：

D O I：

10.1016/j.nmd.2010.07.107

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

引用

页码：629 / 629

页数：1

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