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3. Hereditary folate malabsorption: a positively charged amino acid at position 113 of the proton-coupled folate transporter (PCFT/SLC46A1) is required for folic acid binding. Lasry I; Berman B; Glaser F; Jansen G; Assaraf YG Biochem Biophys Res Commun; 2009 Aug; 386(3):426-31. PubMed ID: 19508863 [TBL] [Abstract][Full Text] [Related]
4. A novel deletion mutation in the proton-coupled folate transporter (PCFT; SLC46A1) in a Nicaraguan child with hereditary folate malabsorption. Diop-Bove N; Jain M; Scaglia F; Goldman ID Gene; 2013 Sep; 527(2):673-4. PubMed ID: 23816405 [TBL] [Abstract][Full Text] [Related]
7. Mutation of the proton-coupled folate transporter gene (PCFT-SLC46A1) in Turkish siblings with hereditary folate malabsorption. Atabay B; Turker M; Ozer EA; Mahadeo K; Diop-Bove N; Goldman ID Pediatr Hematol Oncol; 2010 Nov; 27(8):614-9. PubMed ID: 20795774 [TBL] [Abstract][Full Text] [Related]
8. A family study of congenital malabsorption of folate. Jebnoun S; Kacem S; Mokrani CH; Chabchoub A; Khrouf N; Zittoun J J Inherit Metab Dis; 2001 Dec; 24(7):749-50. PubMed ID: 11804211 [No Abstract] [Full Text] [Related]
9. Malabsorption. Finkelstein JD Med Clin North Am; 1968 Nov; 52(6):1339-54. PubMed ID: 4886056 [No Abstract] [Full Text] [Related]
10. Congenital malabsorption of folate. Lanzkowsky P Am J Med; 1970 May; 48(5):580-3. PubMed ID: 5450108 [No Abstract] [Full Text] [Related]
11. Importance of vitamin B12 and folate metabolism in malabsorption. Gallagher ND Clin Gastroenterol; 1983 May; 12(2):437-41. PubMed ID: 6347465 [TBL] [Abstract][Full Text] [Related]
12. The clinical course and genetic defect in the PCFT gene in a 27-year-old woman with hereditary folate malabsorption. Min SH; Oh SY; Karp GI; Poncz M; Zhao R; Goldman ID J Pediatr; 2008 Sep; 153(3):435-7. PubMed ID: 18718264 [TBL] [Abstract][Full Text] [Related]
13. Isolated congenital malabsorption of folic acid in a male infant: insights into treatment and mechanism of defect. Malatack JJ; Moran MM; Moughan B Pediatrics; 1999 Nov; 104(5 Pt 1):1133-7. PubMed ID: 10545560 [TBL] [Abstract][Full Text] [Related]
14. Identification of proton-coupled high-affinity human intestinal folate transporter mutated in human hereditary familial folate malabsorption. Wolf G Nutr Rev; 2007 Dec; 65(12 Pt 1):554-7. PubMed ID: 18236695 [TBL] [Abstract][Full Text] [Related]
16. Additional information on congenital defect in absorption of folic acid. Santini R; Millán S; Santiago-Borrero PJ J Pediatr; 1973 Aug; 83(2):345-6. PubMed ID: 4717594 [No Abstract] [Full Text] [Related]
17. The spectrum of mutations in the PCFT gene, coding for an intestinal folate transporter, that are the basis for hereditary folate malabsorption. Zhao R; Min SH; Qiu A; Sakaris A; Goldberg GL; Sandoval C; Malatack JJ; Rosenblatt DS; Goldman ID Blood; 2007 Aug; 110(4):1147-52. PubMed ID: 17446347 [TBL] [Abstract][Full Text] [Related]
18. Intestinal methylation of folates. Baker H; Frank O Lancet; 1969 Nov; 2(7630):1135-6. PubMed ID: 4188075 [No Abstract] [Full Text] [Related]