P.9.2 Autosomal dominant nemaline myopathy with marked...

Neuromuscular Disorders 2013 / 10 Vol. 23; Iss. 9-10

P.9.2 Autosomal dominant nemaline myopathy with marked intrafamilial phenotypic variability

Park, J.S., Shin, J.H., Hwang, S.J., Kim, D.S.
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Volume:
23
Language:
english
Journal:
Neuromuscular Disorders
DOI:
10.1016/j.nmd.2013.06.515
Date:
October, 2013
File:
PDF, 57 KB
english, 2013
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