The Hemochromatosis Founder Mutation in HLA-H Disrupts β2-Microglobulin Interaction and Cell Surface Expression-Reference-Cited by-同舟云学术

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The Hemochromatosis Founder Mutation in HLA-H Disrupts β2-Microglobulin Interaction and Cell Surface Expression

Published:1997-05 Issue:22 Volume:272 Page:14025-14028
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Feder John N.,Tsuchihashi Zenta,Irrinki Alivelu,Lee Vincent K.,Mapa Felipa A.,Morikang Ebenezer,Prass Cynthia E.,Starnes Steven M.,Wolff Roger K.,Parkkila Seppo,Sly William S.,Schatzman Randall C.

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference22 articles.

1. Hereditary Hemochromatosis: Analysis of Laboratory Expression of the Disease by Genotype in 18 Pedigrees

2. Prevalence of Hemochromatosis among 11,065 Presumably Healthy Blood Donors

3. A novel MHC class I–like gene is mutated in patients with hereditary haemochromatosis

4. Haemochromatosis and HLA–H

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