The biochemical and clinical penetrance of individuals diagnosed with genetic haemochromatosis by predictive genetic testing-Reference-Cited by-同舟云学术

The biochemical and clinical penetrance of individuals diagnosed with genetic haemochromatosis by predictive genetic testing

Published:2008-05 Issue:5 Volume:20 Page:379-383
ISSN:0954-691X
Container-title:European Journal of Gastroenterology & Hepatology
language:en
Short-container-title:European Journal of Gastroenterology & Hepatology

Author:

Watkins Stuart,Thorburn Douglas,Joshi Neeraj,Neilson Margaret,Joyce Theresa,Spooner Richard,Cooke Alexander,Mills Peter R.,Morris A. John,Stanley Adrian J.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Gastroenterology,Hepatology

Reference24 articles.

1. EASL International Consensus Conference on Haemochromatosis

2. Original Paper: Hereditary haemochromatosis and hepatocellular carcinoma in males: a strategy for estimating the potential for primary prevention

3. Early onset hereditary hemochromatosis resulting from a novel TFR2 gene nonsense mutation (R105X) in two siblings of north French descent

4. Digenic inheritance of mutations in HAMP and HFE results in different types of haemochromatosis

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