Congenital Myasthenic Syndrome due to a Novel Mutation in CHAT Gene.
Autor: | Dhasakeerthi, Thirumalaivasan, Aravindhan, Akilandeswari, Woodall, Aaron, Mills, Weston, Veerapandiyan, Aravindhan |
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Zdroj: | Journal of Clinical Neuromuscular Disease; Sep2021, Vol. 23 Issue 1, p54-55, 2p |
Databáze: | Complementary Index |
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