Title : Analysis of slc19a2, on 1q23.3 encoding a thiamine transporter as a candidate gene for type 2 diabetes mellitus in pima indians.

Pub. Date : 2001 Apr

PMID : 11286512






2 Functional Relationships(s)
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Sentence
Compound Name
Protein Name
Organism
1 Mutations in the SLC19A2 gene cause thiamine-responsive megaloblastic anemia (TRMA) frequently combined with diabetes mellitus and deafness. Thiamine solute carrier family 19 member 2 Homo sapiens
2 Mutations in the SLC19A2 gene cause thiamine-responsive megaloblastic anemia (TRMA) frequently combined with diabetes mellitus and deafness. Thiamine solute carrier family 19 member 2 Homo sapiens