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pro vyhledávání: '"Maya Soufan"'
Publikováno v:
American Journal of Perinatology Reports, Vol 14, Iss 03, Pp e193-e196 (2024)
Congenital myasthenia gravis syndrome (CMS) is a rare genetic heterogeneous disorder due to abnormal neuromuscular transmission caused by several genes. CMS caused by choline acetyltransferase (ChAT) gene mutations have been reported in 53 cases sinc
Externí odkaz:
https://doaj.org/article/374cee4b1ed34c888de78712a146b60c
