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[Two cases of hepatolenticular degeneration caused by combined R778L and P992L mutation].
Cheng, Q Q; Yang, L X; Xu, Q L; Yan, X H; Wu, X P; Ge, S F.
Afiliação
  • Cheng QQ; Department of Infectious Diseases, The First Affiliated Hospital of Nanchang University, Nanchang 330006, China.
  • Yang LX; Department of Infectious Diseases, The First Affiliated Hospital of Nanchang University, Nanchang 330006, China.
  • Xu QL; Department of Infectious Diseases, The First Affiliated Hospital of Nanchang University, Nanchang 330006, China.
  • Yan XH; Department of Infectious Diseases, Shangrao Second People's Hospital, Shangrao 334000, China.
  • Wu XP; Department of Infectious Diseases, The First Affiliated Hospital of Nanchang University, Nanchang 330006, China.
  • Ge SF; Department of Infectious Diseases, The First Affiliated Hospital of Nanchang University, Nanchang 330006, China.
Zhonghua Gan Zang Bing Za Zhi ; 29(12): 1201-1204, 2021 Dec 20.
Article em Zh | MEDLINE | ID: mdl-35045639

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Degeneração Hepatolenticular Limite: Humans Idioma: Zh Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Degeneração Hepatolenticular Limite: Humans Idioma: Zh Ano de publicação: 2021 Tipo de documento: Article