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.
Citación estilo ChicagoShin, Daniel Sanghoon, Rongbao Zhao, Andras Fiser, y 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.
Cita MLAShin, Daniel Sanghoon, Rongbao Zhao, Andras Fiser, y 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.