Shin, D. S., Mahadeo, K., Min, S. H., Diop-Bove, N., Clayton, P., Zhao, R., & Goldman, I. D. (2011). Identification of novel mutations in the proton-coupled folate transporter (PCFT-SLC46A1) associated with hereditary folate malabsorption.

Shin, Daniel Sanghoon, Kris Mahadeo, Sang Hee Min, Ndeye Diop-Bove, Peter Clayton, Rongbao Zhao, và I. David Goldman. Identification of Novel Mutations in the Proton-coupled Folate Transporter (PCFT-SLC46A1) Associated With Hereditary Folate Malabsorption. 2011.

Shin, Daniel Sanghoon, et al. Identification of Novel Mutations in the Proton-coupled Folate Transporter (PCFT-SLC46A1) Associated With Hereditary Folate Malabsorption. 2011.