O.21 Congenital Myasthenic Syndrome (CMS), autophagic...

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

O.21 Congenital Myasthenic Syndrome (CMS), autophagic myopathy, and cognitive dysfunction caused by mutations in DPAGT1

Selcen, D., Shen, X.M., Li, Y., Wieben, E.D., Engel, A.G.
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Volume:
23
Language:
english
Journal:
Neuromuscular Disorders
DOI:
10.1016/j.nmd.2013.06.731
Date:
October, 2013
File:
PDF, 48 KB
english, 2013
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