Title : Thiamine transporter mutation: an example of monogenic diabetes mellitus.

Pub. Date : 2006 Dec

PMID : 17132746






2 Functional Relationships(s)
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Sentence
Compound Name
Protein Name
Organism
1 OBJECTIVE: Thiamine-responsive megaloblastic anemia (TRMA) is a rare syndrome characterized by diabetes mellitus (DM), anemia, and sensorineural deafness. Thiamine solute carrier family 19 member 2 Homo sapiens
2 A diagnosis of TRMA was suspected and the patient was treated with thiamine hydrochloride. THIAMINE HYDROCHLORIDE solute carrier family 19 member 2 Homo sapiens