Identification of four SLC19A2 mutations in four Chinese thiamine responsive megaloblastic anemia patients without diabetes
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Hematology,Molecular Biology,Molecular Medicine
Reference8 articles.
1. Ring sideroblasts and sideroblastic anemias;Cazzola;Haematologica,2011
2. Hereditary sideroblastic anemia: pathophysiology and gene mutations;Harigae;Int. J. Hematol.,2010
3. Thiamine-responsive megaloblastic anemia: identification of novel compound heterozygotes and mutation update;Bergmann;J. Pediatr.,2009
4. TRMA syndrome (thiamine‐responsive megaloblastic anemia): a case report and review of the literature;Ozdemir;Pediatr. Diabetes,2002
5. The gene mutated in thiamine-responsive anaemia with diabetes and deafness (TRMA) encodes a functional thiamine transporter;Fleming;Nat. Genet.,1999
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