Iron metabolism in heterozygotes for hemoglobin E (HbE), α-thalassemia 1, or β-thalassemia and in compound heterozygotes for HbE/β-thalassemia-Reference-Cited by-同舟云学术

Iron metabolism in heterozygotes for hemoglobin E (HbE), α-thalassemia 1, or β-thalassemia and in compound heterozygotes for HbE/β-thalassemia

Published:2008-10-01 Issue:4 Volume:88 Page:1026-1031
ISSN:0002-9165
Container-title:The American Journal of Clinical Nutrition
language:en
Short-container-title:

Author:

Zimmermann Michael B¹,Fucharoen Suthat¹,Winichagoon Pattanee¹,Sirankapracha Pornpan¹,Zeder Christophe¹,Gowachirapant Sueppong¹,Judprasong Kunchit¹,Tanno Toshihiko¹,Miller Jeffery L¹,Hurrell Richard F¹

Affiliation:

1. From the Laboratory for Human Nutrition, Swiss Federal Institute of Technology Zürich, Zürich, Switzerland (MBZ, CZ, and RFH); the Thalassemia Research Center, Institute of Science and Technology for Research and Development (SF and PS) and the Institute of Nutrition (PW, SG, and KJ), Mahidol University, Salaya, Nakon Pathom, Thailand; and the Molecular Medicine Branch, National Institute of Diab

Publisher

Oxford University Press (OUP)

Subject

Nutrition and Dietetics,Medicine (miscellaneous)

Link

http://academic.oup.com/ajcn/article-pdf/88/4/1026/23920871/znu01008001026.pdf

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4. Iron absorption and loading in beta-thalassaemia intermedia;Pippard;Lancet,1979

5. A correlation of erythrokinetics, ineffective erythropoiesis, and erythroid precursor apoptosis in Thai patients with thalassemia;Pootrakul;Blood,2000

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