Title : Analysis of thiamine transporter genes in sporadic beriberi.

Pub. Date : 2014 Apr

PMID : 24607307






1 Functional Relationships(s)
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1 We analyzed for the first time, the role of all known mutations within three specific thiamine carrier genes, SLC19 A2, SLC19 A3, and SLC25 A19, in a patient with atrophic beriberi, a multiorgan nutritional disease caused by thiamine deficiency. Thiamine solute carrier family 19 member 3 Homo sapiens