A Case of Congenital Myasthenia Gravis due to ChAT Gene Mutation in a Term Neonate: A Case Report
AJP Rep. 2024 Jul 19;14(3):e193-e196. doi: 10.1055/a-2363-6319. eCollection 2024 Jul. ABSTRACT Congenital myasthenia gravis syndrome (CMS) is a rare genetic heterogeneous disorder due to abnormal …