Mahadeo, K., Diop-Bove, N., Shin, D., Unal, E. S., Teo, J., Zhao, R., . . . Goldman, I. D. (2010). Properties of the Arg376 residue of the proton-coupled folate transporter (PCFT-SLC46A1) and a glutamine mutant causing hereditary folate malabsorption. American Physiological Society.
Dyfyniad Arddull ChicagoMahadeo, Kris, et al. Properties of the Arg376 Residue of the Proton-coupled Folate Transporter (PCFT-SLC46A1) and a Glutamine Mutant Causing Hereditary Folate Malabsorption. American Physiological Society, 2010.
Dyfyniad MLAMahadeo, Kris, et al. Properties of the Arg376 Residue of the Proton-coupled Folate Transporter (PCFT-SLC46A1) and a Glutamine Mutant Causing Hereditary Folate Malabsorption. American Physiological Society, 2010.
Rhybudd: Mae'n bosib nad yw'r dyfyniadau hyn bob amser yn 100% cywir.