[Phenotype and genotype analysis of 55 children patients with Wilson's disease].

Zhou, X Y; Yin, H X; Wang, C L; Liu, Z F; Zheng, B X; Jin, Y

Zhou, X Y; Yin, H X; Wang, C L; Liu, Z F; Zheng, B X; Jin, Y.

Afiliação

Zhou XY; Department of Gastroenterology, the Affiliated Children's Hospital of Nanjing Medical University, Nanjing 210008, China.
Yin HX; Department of Gastroenterology, the Affiliated Children's Hospital of Nanjing Medical University, Nanjing 210008, China.
Wang CL; Department of Gastroenterology, the Affiliated Children's Hospital of Nanjing Medical University, Nanjing 210008, China.
Liu ZF; Department of Gastroenterology, the Affiliated Children's Hospital of Nanjing Medical University, Nanjing 210008, China.
Zheng BX; Department of Gastroenterology, the Affiliated Children's Hospital of Nanjing Medical University, Nanjing 210008, China.
Jin Y; Department of Gastroenterology, the Affiliated Children's Hospital of Nanjing Medical University, Nanjing 210008, China.

Zhonghua Gan Zang Bing Za Zhi ; 28(7): 603-607, 2020 Jul 20.

Article em Zh | MEDLINE | ID: mdl-32791797

Assuntos

ATPases Transportadoras de Cobre/genética; Degeneração Hepatolenticular; Criança; China; Análise Mutacional de DNA; Genótipo; Degeneração Hepatolenticular/genética; Humanos; Mutação; Fenótipo; Análise de Sequência de DNA

Palavras-chave

ATP7B; Genes and phenotypes; Long fragment deletion mutation; Wilson disease

Texto completo

Adicionar na Minha BVS

Imprimir

XML

PubMed Links

Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: ATPases Transportadoras de Cobre / Degeneração Hepatolenticular Limite: Child / Humans País/Região como assunto: Asia Idioma: Zh Revista: Zhonghua Gan Zang Bing Za Zhi Assunto da revista: GASTROENTEROLOGIA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: China País de publicação: China

Texto completo

Adicionar na Minha BVS

Imprimir

XML

PubMed Links

Buscar no Google