The Clinical Course and Genetic Defect in the PCFT Gene in a 27-Year-Old Woman with Hereditary Folate Malabsorption
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology and Child Health
Reference11 articles.
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2. Inherited disorders of folate and cobalamin transport and metabolism;Rosenblatt,2001
3. 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
4. Identification of an intestinal folate transporter and the molecular basis for hereditary folate malabsorption;Qiu;Cell,2006
5. Therapy of congenital folate malabsorption;Poncz;J Pediatr,1981
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