Hereditary inclusion body myopathy with a novel mutation in the GNE gene associated with proximal leg weakness and necrotizing myopathy

被引：14
作者：
Motozaki, Y.
Komai, K.
Hirohata, M.
Asaka, T.
Ono, K.
Yamada, M.
机构：
[1] Kanazawa Univ, Grad Sch Med Sci, Dept Neurol & Neurobiol Aging, Kanazawa, Ishikawa 9208641, Japan
[2] Nanao Natl Hosp, Dept Neurol, Nanao, Japan
来源：
EUROPEAN JOURNAL OF NEUROLOGY | 2007年 / 14卷 / 09期
关键词：
GNE mutation; hereditary inclusion body myopathy; necrotizing myopathy; proximal weakness; rimmed vacuole;
D O I：
10.1111/j.1468-1331.2007.01905.x
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
引用
收藏
页码：E14 / E15
页数：2
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