Hereditary folate malabsorption with a novel mutation on SLC46A1
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
General Medicine
Reference12 articles.
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2. Identification of an intestinal folate transporter and the molecular basis for hereditary folate malabsorption;Qiu;Cell,2006
3. The proton-coupled folate transporter (PCFT-SLC46A1) and the syndrome of systemic and cerebral folate deficiency of infancy: hereditary folate malabsorption;Zhao;Mol Aspects Med,2017
4. The human proton-coupled folate transporter: biology and therapeutic applications to cancer;Desmoulin;Cancer Biol Ther,2012
5. The spectrum of mutations in the PCFT gene, coding for an intestinal folate transporter, that are the basis for hereditary folate malabsorption;Zhao;Blood,2007
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