Clinical presentation and mutations in Danish patients with Wilson disease-Reference-Cited by-同舟云学术

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Clinical presentation and mutations in Danish patients with Wilson disease

Published:2011-05-25 Issue:9 Volume:19 Page:935-941
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Møller Lisbeth Birk,Horn Nina,Jeppesen Tina Dysgaard,Vissing John,Wibrand Flemming,Jennum Poul,Ott Peter

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://www.nature.com/articles/ejhg201180.pdf

Reference41 articles.

1. Roberts EA, Schilsky ML : Diagnosis and treatment of Wilson disease: an update. Hepatology 2008; 47: 2089–2111.

2. Olsson C, Waldenstrom E, Westermark K, Landegre U, Syvanen AC : Determination of the frequencies of ten allelic variants of the Wilson disease gene (ATP7B), in pooled DNA samples. Eur J Hum Genet 2000; 8: 933–938.

3. Gitlin N : Wilson's disease: the scourge of copper. J Hepatol 1998; 28: 734–739.

4. Ala A, Walker AP, Ashkan K, Dooley JS, Schilsky ML : Wilson's disease. Lancet 2007; 369: 397–408.

5. Turnlund JR : Human whole-body copper metabolism. Am J Clin Nutr 1998; 67 (5 Suppl): 960S–964S.

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