Diop-Bove, N., Jain, M., Scaglia, F., & Goldman, I. (2013). A novel deletion mutation in the proton-coupled folate transporter (PCFT; SLC46A1) in a Nicaraguan child with hereditary folate malabsorption.
Citación estilo ChicagoDiop-Bove, N., M. Jain, F. Scaglia, and I.D Goldman. A Novel Deletion Mutation in the Proton-coupled Folate Transporter (PCFT; SLC46A1) in a Nicaraguan Child With Hereditary Folate Malabsorption. 2013.
Cita MLADiop-Bove, N., M. Jain, F. Scaglia, and I.D Goldman. A Novel Deletion Mutation in the Proton-coupled Folate Transporter (PCFT; SLC46A1) in a Nicaraguan Child With Hereditary Folate Malabsorption. 2013.
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