Title : A novel mutation in the SLC19A2 gene in a Turkish female with thiamine-responsive megaloblastic anemia syndrome.

Pub. Date : 2009 Aug

PMID : 18614593






2 Functional Relationships(s)
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1 A novel mutation in the SLC19A2 gene in a Turkish female with thiamine-responsive megaloblastic anemia syndrome. Thiamine solute carrier family 19 member 2 Homo sapiens
2 Besides reporting a new mutation on the gene SLC19A2 for the first time in the literature, we highlight the recognition of this syndrome--when megaloblastic anemia and diabetes mellitus coexists--and the role of thiamine replacement for the treatment of both disorders. Thiamine solute carrier family 19 member 2 Homo sapiens