Shin, D. S., Zhao, R., Fiser, A., & Goldman, D. I. (2012). Functional roles of the A335 and G338 residues of the proton-coupled folate transporter (PCFT-SLC46A1) mutated in hereditary folate malabsorption. American Physiological Society.
Chicago Style CitationShin, Daniel Sanghoon, Rongbao Zhao, Andras Fiser, and David I. Goldman. Functional Roles of the A335 and G338 Residues of the Proton-coupled Folate Transporter (PCFT-SLC46A1) Mutated in Hereditary Folate Malabsorption. American Physiological Society, 2012.
MLA CitationShin, Daniel Sanghoon, Rongbao Zhao, Andras Fiser, and David I. Goldman. Functional Roles of the A335 and G338 Residues of the Proton-coupled Folate Transporter (PCFT-SLC46A1) Mutated in Hereditary Folate Malabsorption. American Physiological Society, 2012.