AB088. Mutation analysis of 16 Vietnamses Wilson patients

BACKGROUND: Wilson disease (WD) is an autosomal recessive disorder of copper transport, which is caused by mutation in copper-transporting P-type ATPase (ATP7B). OBJECTIVE: The aim of this study was to detect mutations in hot-spot region of ATP7B gene, including exon 2b, 8, 11, 12, and 13. Sixteen u...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:Ann Transl Med
Main Authors: Nguyen, Thi Mai Hương, Ngoc, Ngo Diem, Nguyen, Thi Phương Mai, Hoa, Nguyen Pham Anh, Khánh, Trần Vân, Văn, Tạ Thành, Chi, Phan Van
Formato: Artigo
Idioma:Inglês
Publicado em: AME Publishing Company 2015
Assuntos:
Part 4: Oral/poster
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4563458/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3978/j.issn.2305-5839.2015.AB088
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados