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

Published 2010 View Full Article

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Title
A novel ACTA1 mutation resulting in a severe congenital myopathy with nemaline bodies, intranuclear rods and type I fibre predominance
Authors
Keywords
-
Journal
NEUROMUSCULAR DISORDERS
Volume 21, Issue 1, Pages 31-36
Publisher
Elsevier BV
Online
2010-09-18
DOI
10.1016/j.nmd.2010.08.005

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