Prevalence of ATP7B Gene Mutations in Iranian Patients With Wilson Disease-Reference-Cited by-同舟云学术

Prevalence of ATP7B Gene Mutations in Iranian Patients With Wilson Disease

Published:2011-11-01 Issue:11 Volume:11 Page:890-894
ISSN:1735-143X
Container-title:Hepatitis Monthly
language:
Short-container-title:Hepat Mon

Author:

Zali Narges,Mohebbi Seyed Reza,Esteghamat Sahar,Chiani Mohsen,Haghighi Mahdi Montazer,Hosseini-Asl Seyed Mohammad-Kazem,Derakhshan Faramarz,Mohammad-Alizadeh Amir-Houshang,Malek-Hosseini Seyed-Ali,Zali Mohammad Reza

Publisher

Briefland

Subject

Infectious Diseases,Hepatology

Reference20 articles.

1. Mutation analysis of Wilson disease in the Spanish population - identification of a prevalent substitution and eight novel mutations in the ATP7B gene

2. The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene

3. Long Range Restriction Mapping of 13q14.3 Focused on the Wilson Disease Region

4. His1069Gln and six novel Wilson disease mutations: analysis of relevance for early diagnosis and phenotype

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