Clinical features and gene mutation analysis of severe congenital nemaline myopathy in one neonate.
- Author:
Xiang-Wen HU
1
;
Wen-Yan TANG
;
Ju-Mei GAO
Author Information
- Publication Type:Journal Article
- MeSH: Humans; Infant, Newborn; Muscle Proteins; Muscle, Skeletal; Mutation; Myopathies, Nemaline
- From: Chinese Journal of Contemporary Pediatrics 2019;21(5):497-498
- CountryChina
- Language:Chinese
