ABC of D's in the folate transporter
- PMID: 21148336
- DOI: 10.1182/blood-2010-09-306381
ABC of D's in the folate transporter
Comment on
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Functional roles of aspartate residues of the proton-coupled folate transporter (PCFT-SLC46A1); a D156Y mutation causing hereditary folate malabsorption.Blood. 2010 Dec 9;116(24):5162-9. doi: 10.1182/blood-2010-06-291237. Epub 2010 Aug 30. Blood. 2010. PMID: 20805364 Free PMC article.
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