O.22 Autosomal dominant Core Congenital Myopathy caused by...

O.22 Autosomal dominant Core Congenital Myopathy caused by a mutation in the MYH7 gene

Romero, N.B., Xie, T., Malfatti, E., Schaeffer, U., Fardeau, M., Laporte, J.
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Volume:
23
Language:
english
Journal:
Neuromuscular Disorders
DOI:
10.1016/j.nmd.2013.06.732
Date:
October, 2013
File:
PDF, 47 KB
english, 2013
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