A homozygous HFE gene splice site mutation (IVS5+1 G/A) in a hereditary hemochromatosis patient of Vietnamese origin-Reference-Cited by-同舟云学术

A homozygous HFE gene splice site mutation (IVS5+1 G/A) in a hereditary hemochromatosis patient of Vietnamese origin

Published:2002-03 Issue:3 Volume:122 Page:789-795
ISSN:0016-5085
Container-title:Gastroenterology
language:en
Short-container-title:Gastroenterology

Author:

Steiner Michael,Ocran Kenneth,Genschel Janine,Meier Patrick,Gerl Helga,Ventz Michael,Schneider Marie-Luise,Büttner Carsten,Wadowska Kamilla,Kerner Wolfgang,Schuff–Werner Peter,Lochs Herbert,Schmidt Hartmut

Publisher

Elsevier BV

Subject

Gastroenterology,Hepatology

Reference30 articles.

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3. A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis;Feder;Nat Genet,1996

4. Phenotype-genotype correlation in haemochromatosis subjects;Mura;Hum Genet,1997

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