Neonatal Congenital Myasthenic Syndrome Linked to CHAT Gene Variants: A Case Report and Treatment Insights
新生儿先天性肌无力综合征与CHAT基因变异相关：病例报告及治疗见解
期刊:American Journal of Case Reports
影响因子:0.7
doi:10.12659/AJCR.946839
Khalil, Mohammed Rohi; Laulund, Lone Walentin; Aavild Ploug, Anna Julie; Elle, Ida Coordt; Fenger-Groen, Jesper
