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Limb-girdle muscular dystrophy related to LAMA2 mutations: an unusual familial coincidence responsible for the phenotypic variability and diagnostic difficulties
Guillet-Pichon, V., Leturcq, F., Claeys, K., Beroud, C., Nadaj-Pakleza, A.Volume:
27
Language:
english
Journal:
Neuromuscular Disorders
DOI:
10.1016/j.nmd.2017.06.064
Date:
October, 2017
File:
PDF, 239 KB
english, 2017