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Items: 3

1.
Identification of novel mutations in the proton-coupled folate transporter (PCFT-SLC46A1) associated with hereditary folate malabsorption
Daniel Sanghoon Shin, Kris Mahadeo, Sang Hee Min, Ndeye Diop-Bove, Peter Clayton, Rongbao Zhao, I. David Goldman
Mol Genet Metab. Author manuscript; available in PMC 2012 May 1.
Published in final edited form as: Mol Genet Metab. 2011 May; 103(1): 33–37. Published online 2011 Jan 25. doi: 10.1016/j.ymgme.2011.01.008
PMCID:
PMC3081934
AbstractArticlePDF–576K
2.
The spectrum of mutations in the PCFT gene, coding for an intestinal folate transporter, that are the basis for hereditary folate malabsorption
Rongbao Zhao, Sang Hee Min, Andong Qiu, Antoinette Sakaris, Gary L. Goldberg, Claudio Sandoval, J. Jeffrey Malatack, David S. Rosenblatt, I. David Goldman
Blood. 2007 Aug 15; 110(4): 1147–1152. Prepublished online 2007 Apr 19. doi: 10.1182/blood-2007-02-077099
PMCID:
PMC1939898
AbstractArticle
3.
Congenital isolated folic acid malabsorption.
J Urbach, A Abrahamov, N Grossowicz
Arch Dis Child. 1987 Jan; 62(1): 78–80. doi: 10.1136/adc.62.1.78
PMCID:
PMC1778153
SummaryPage BrowsePDF–419K

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