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The first Chinese case report of hereditary folate malabsorption with a novel mutation on SLC46A1

  • Published:2015-01 Issue:1 Volume:37 Page:163-167
  • ISSN:0387-7604
  • Container-title:Brain and Development
  • language:en
  • Short-container-title:Brain and Development

Author:

Wang Qiao,Li Xiyuan,Ding Yuan,Liu Yupeng,Qin Yaping,Yang Yanling

Funder

National Nature Science Foundation of China

Publisher

Elsevier BV

Subject

Neurology (clinical),Developmental Neuroscience,General Medicine,Pediatrics, Perinatology and Child Health

Reference13 articles.

1. Inherited disorders of folate and cobalamin transport and metabolism;Rosenblatt,2001

2. Identification of an intestinal folate transporter and the molecular basis for hereditary folate malabsorption;Qiu;Cell,2006

3. Characterization of folate uptake by choroid plexus epithelial cells in a rat primary culture model;Wollack;J Neurochem,2008

4. Hereditary folate malabsorption;Ndeye,1993

5. Hereditary folate malabsorption: family report and review of the literature;Geller;Medicine (Baltimore),2002

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