Mild dehydrated hereditary stomatocytosis revealed by marked hepatosiderosis
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2257.2006.00774.x/fullpdf
Reference20 articles.
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2. Two new human DMT1 mutations in a compound heterozygous patient with microcytic anemia and low iron stores;Beaumont;Blood,2006
3. The significance of the 187G (H63D) mutation in hemochromatosis;Beutler;American Journal of Human Genetics,1997
4. The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22;Camaschella;Nature Genetics,2000
5. Genomewide search for dehydrated hereditary stomatocytosis (hereditary xerocytosis): mapping of locus to chromosome 16 (16q23-qter);Carella;American Journal of Human Genetics,1998
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