Study on Mutation in Exon 8 of ATP7B Gene in Chinese Patients with Wilson Disease / 实用儿科临床杂志
Journal of Applied Clinical Pediatrics
; (24)2004.
Article
em Zh
| WPRIM
| ID: wpr-639926
Biblioteca responsável:
WPRO
ABSTRACT
G,the noval insertion mutation of c.2298_2299insC is identified in Chinese patients.
Texto completo:
1
Base de dados:
WPRIM
Idioma:
Zh
Revista:
Journal of Applied Clinical Pediatrics
Ano de publicação:
2004
Tipo de documento:
Article