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Homozygous MYH7 R1820W mutation results in recessive myosin storage myopathy: Scapuloperoneal and respiratory weakness with dilated cardiomyopathy
Yüceyar, Nur, Ayhan, Özgecan, Karasoy, Hatice, Tolun, AslıhanVolume:
25
Language:
english
Journal:
Neuromuscular Disorders
DOI:
10.1016/j.nmd.2015.01.007
Date:
April, 2015
File:
PDF, 351 KB
english, 2015