Mutation analysis of transferrin-receptor 2 in patients with atypical hemochromatosis-Reference-Cited by-同舟云学术

Mutation analysis of transferrin-receptor 2 in patients with atypical hemochromatosis

Published:2002-08-01 Issue:3 Volume:100 Page:1099-1100
ISSN:1528-0020
Container-title:Blood
language:en
Short-container-title:

Author:

Hofmann Wolf-K.¹,Tong Xiang-Jun¹,Ajioka Richard S.¹,Kushner James P.¹,Koeffler H. Phillip¹

Affiliation:

1. Correspondence: Wolf-K. Hofmann, Division of Hematology/Oncology, Cedars Sinai Research Institute, UCLA School of Medicine, Los Angeles, CA 90048; e-mail:

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Link

http://ashpublications.org/blood/article-pdf/100/3/1099/1684713/h81502001092e.pdf

Reference8 articles.

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

2. Molecular cloning of transferrin receptor 2: a new member of the transferrin receptor-like family.;Kawabata;J Biol Chem.,1999

3. The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22.;Camaschella;Nat Genet.,2000

4. TFR2 Y250X mutation in Italy.;De Gobbi;Br J Haematol.,2001

5. New mutations inactivating transferrin receptor 2 in hemochromatosis type 3.;Roetto;Blood.,2001

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