Detalhe da pesquisa
1.
SCN4A-related congenital myopathy in a Han Chinese patient: A case report and literature review.
Heliyon
; 10(1): e23663, 2024 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-38187266
2.
Founder Mutation c.1516A>C in KLHL40 Is a Frequent Cause of Nemaline Myopathy With Hyponatremia in Ethnic Chinese.
J Neuropathol Exp Neurol
; 78(9): 854-864, 2019 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31360996