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Classic congenital myopathy with recessive mutations in genes encoding ion channels: clinical phenotype and good response to acetazolamide
Munot, P., Zaharieva, I., Hartley, L., Phadke, R., Sewry, C., Feng, L., Sud, R., Hanna, M., Matthews, E., Muntoni, F.Volume:
27
Language:
english
Journal:
Neuromuscular Disorders
DOI:
10.1016/j.nmd.2017.06.333
Date:
October, 2017
File:
PDF, 240 KB
english, 2017