DNA haplotype analysis for the diagnosis of Wilson disease in siblings-Reference-Cited by-同舟云学术

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DNA haplotype analysis for the diagnosis of Wilson disease in siblings

Published:2007-01-02 Issue:9 Volume:89 Page:1142-1144
ISSN:0803-5253
Container-title:Acta Paediatrica
language:en
Short-container-title:

Author:

Yüce A,Koçak N,Demirtas M,Özen H,Gürakan F,Özgüç M

Publisher

Wiley

Subject

General Medicine,Pediatrics, Perinatology and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1651-2227.2000.tb03367.x/fullpdf

Reference14 articles.

1. Wilson's disease patients with normal ceruloplasmin levels;Yüce;Turk J Pediatr,1999

2. Wilson disease in 1998: genetic, diagnostic and therapeutic aspect;Gollan;J Hepatol,1998

3. Wilson's disease;Ferenci;Clin Liv Dis,1998

4. The Wilson's disease gene: spectrum of mutations and their consequences;Thomas;Nat Genet,1995

5. Diagnosis of Wilson's disease in an asymptomatic sibling by DNA linkage analysis;Maier-Dobersberger;Gastroenterology,1995

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Bone mineralization in children with Wilson’s disease;Indian Journal of Gastroenterology;2014-05-25

2. Haplotype analysis and possible founder effect at the R778L mutation of the ATP7B gene in Korean patients with Wilson's disease;The Korean Journal of Hepatology;2009

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