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Identification of novel mutations in the proton-coupled folate transporter (PCFT-SLC46A1) associated with hereditary folate malabsorption.
Mol Genet Metab. 2011 May;103(1):33-7. doi: 10.1016/j.ymgme.2011.01.008. Epub 2011 Jan 25.
Mol Genet Metab. 2011.
PMID: 21333572
Free PMC article.
Vulnerability of the cysteine-less proton-coupled folate transporter (PCFT-SLC46A1) to mutational stress associated with the substituted cysteine accessibility method.
Zhao R, Shin DS, Goldman ID.
Zhao R, et al.
Biochim Biophys Acta. 2011 Apr;1808(4):1140-5. doi: 10.1016/j.bbamem.2011.01.008. Epub 2011 Jan 20.
Biochim Biophys Acta. 2011.
PMID: 21256110
Free PMC article.
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