Congenital Myasthenic Syndrome due to a Novel Mutation in CHAT Gene.

Autor: Dhasakeerthi, Thirumalaivasan, Aravindhan, Akilandeswari, Woodall, Aaron, Mills, Weston, Veerapandiyan, Aravindhan
Zdroj: Journal of Clinical Neuromuscular Disease; Sep2021, Vol. 23 Issue 1, p54-55, 2p
Databáze: Complementary Index