A novel ACTA1 mutation resulting in a severe congenital myopathy with nemaline bodies, intranuclear rods and type I fibre predominance

标题
A novel ACTA1 mutation resulting in a severe congenital myopathy with nemaline bodies, intranuclear rods and type I fibre predominance
作者
关键词
-
出版物
NEUROMUSCULAR DISORDERS
Volume 21, Issue 1, Pages 31-36
出版商
Elsevier BV
发表日期
2010-09-18
DOI
10.1016/j.nmd.2010.08.005

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