Zhao, R., Aluri, S., & Goldman, I. D. (2016). The proton-coupled folate transporter (PCFT-SLC46A1) and the syndrome of systemic and cerebral folate deficiency of infancy: Hereditary folate malabsorption. Mol Aspects Med.
Chicago ZitierstilZhao, Rongbao, Srinivas Aluri, und I. David Goldman. "The Proton-coupled Folate Transporter (PCFT-SLC46A1) and the Syndrome of Systemic and Cerebral Folate Deficiency of Infancy: Hereditary Folate Malabsorption." Mol Aspects Med 2016.
MLA ZitierstilZhao, Rongbao, Srinivas Aluri, und I. David Goldman. "The Proton-coupled Folate Transporter (PCFT-SLC46A1) and the Syndrome of Systemic and Cerebral Folate Deficiency of Infancy: Hereditary Folate Malabsorption." Mol Aspects Med 2016.
Achtung: Diese Zitate sind unter Umständen nicht zu 100% korrekt.