The role of HFE mutations on iron metabolism in beta-thalassemia carriers-Reference-Cited by-同舟云学术

The role of HFE mutations on iron metabolism in beta-thalassemia carriers

Published:2004-11-05 Issue:12 Volume:49 Page:651-655
ISSN:1434-5161
Container-title:Journal of Human Genetics
language:en
Short-container-title:J Hum Genet

Author:

Martins Rute,Picanço Isabel,Fonseca Aidil,Ferreira Lídia,Rodrigues Odete,Coelho Marília,Seixas Teresa,Miranda Armandina,Nunes Baltazar,Costa Luciana,Romão Luísa,Faustino Paula

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://www.nature.com/articles/jhg2004104.pdf

Reference29 articles.

1. Arruda VR, Agostinho MF, Cancado R, Costa FF, Saad ST (2000) Beta-thalassemia trait might increase the severity of hemochromatosis in subjects with the C282Y mutation in the HFE gene. Am J Hematol 63:230–233

2. Asberg A, Thorstensen K, Hveem K, Bjerve KS (2000) Hereditary hemochromatosis: the clinical significance of the S65C mutation. Genet Test 6:59–62

3. Cardoso CS, Oliveira P, Porto G, Oberkanins C, Mascarenhas M, Rodrigues P, Kury F, de Sousa M (2001) Comparative study of the two more frequent HFE mutations (C282Y and H63D): significant different allelic frequencies between the North and South of Portugal. Eur J Hum Genet 9:843–848

4. Cartwright GE, Edwards CQ, Kravitz K, Skolnick M, Amos DB, Johnson A, Buskjaer L (1979) Hereditary hemochromatosis. Phenotypic expression of the disease. N Engl J Med 301:175–179

5. Couto AR, Peixoto MJ, Garrett F, Laranjeira F, Cipriano T, Armas JB (2003) Linkage disequilibrium between S65C HFE mutation and HLA A29-B44 haplotype in Terceira Island, Azores. Hum Immunol 64:625–628

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