A novel ACTA1 mutation resulting in a severe congenital...

Neuromuscular Disorders 2011 Vol. 21; Iss. 1

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

Gianina Ravenscroft, Jo M. Wilmshurst, Komala Pillay, Padma Sivadorai, William Wallefeld, Kristen J. Nowak, Nigel G. Laing
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Volume:
21
Year:
2011
Language:
english
DOI:
10.1016/j.nmd.2010.08.005
File:
PDF, 981 KB
english, 2011
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