Pathophysiology and genetic mutations in congenital sideroblastic anemia
Author:
Affiliation:
1. Department of Hematology and Rheumatology; Tohoku University Graduate School of Medicine; Sendai Japan
2. Molecular Hematology/Oncology; Tohoku University Graduate School of Medicine; Sendai Japan
Publisher
Wiley
Subject
Pediatrics, Perinatology, and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/ped.12217/fullpdf
Reference36 articles.
1. Hereditary sideroblastic anemia: Pathophysiology and gene mutations;Harigae;Int. J. Hematol.,2010
2. Copper deficiency in humans;Williams;Semin. Hematol.,1983
3. Hereditary sideroblastic anemias: Pathophysiology, diagnosis, and treatment;Camaschella;Semin. Hematol.,2009
4. Congenital sideroblastic anemias: Iron and heme lost in mitochondrial translation;Fleming;Hematology Am. Soc. Hematol. Educ. Program,2011
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