Title : TRMA syndrome (thiamine-responsive megaloblastic anemia): a case report and review of the literature.

Pub. Date : 2002 Dec

PMID : 15016149






2 Functional Relationships(s)
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1 TRMA syndrome (thiamine-responsive megaloblastic anemia): a case report and review of the literature. Thiamine solute carrier family 19 member 2 Homo sapiens
2 Thiamine-responsive megaloblastic anemia syndrome (TRMA) is an autosomal recessive disorder with features that include megaloblastic anemia, mild thrombocytopenia and leukopenia, sensorineural deafness and diabetes mellitus. Thiamine solute carrier family 19 member 2 Homo sapiens