Identification of novel mutations in the proton-coupled folate transporter (PCFT-SLC46A1) associated with hereditary folate malabsorption - Concepedia

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Identification of novel mutations in the proton-coupled folate transporter (PCFT-SLC46A1) associated with hereditary folate malabsorption

DOI Full Paper Access

46

Citations

22

References

2011

Year

Daniel Sanghoon Shin, Kris M. Mahadeo, Sang Hee Min, Ndeye Diop-Bove, Peter T. Clayton, Rongbao Zhao, I. David Goldman

Molecular Genetics and Metabolism

Mendelian DisorderBiochemistryNatural SciencesInherited Metabolic DiseaseNovel MutationsBiochemical GeneticsMolecular BiologyHereditary Folate MalabsorptionMetabolismMedicineProton-coupled Folate Transporter

References

	Year	Citations

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