Title : Functional roles of aspartate residues of the proton-coupled folate transporter (PCFT-SLC46A1); a D156Y mutation causing hereditary folate malabsorption.

Pub. Date : 2010 Dec 9

PMID : 20805364






3 Functional Relationships(s)
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1 The proton-coupled folate transporter (PCFT; SLC46A1) mediates folate transport into enterocytes in the proximal small intestine; pcft loss-of-function mutations are the basis for hereditary folate malabsorption. Folic Acid solute carrier family 46 member 1 Homo sapiens
2 The proton-coupled folate transporter (PCFT; SLC46A1) mediates folate transport into enterocytes in the proximal small intestine; pcft loss-of-function mutations are the basis for hereditary folate malabsorption. Folic Acid solute carrier family 46 member 1 Homo sapiens
3 The proton-coupled folate transporter (PCFT; SLC46A1) mediates folate transport into enterocytes in the proximal small intestine; pcft loss-of-function mutations are the basis for hereditary folate malabsorption. Folic Acid solute carrier family 46 member 1 Homo sapiens