The proton-coupled folate transporter (PCFT-SLC46A1) and the syndrome of systemic and cerebral folate deficiency of infancy: Hereditary folate malabsorption-Reference-Cited by-同舟云学术

The proton-coupled folate transporter (PCFT-SLC46A1) and the syndrome of systemic and cerebral folate deficiency of infancy: Hereditary folate malabsorption

Published:2017-02 Issue: Volume:53 Page:57-72
ISSN:0098-2997
Container-title:Molecular Aspects of Medicine
language:en
Short-container-title:Molecular Aspects of Medicine

Author:

Zhao Rongbao,Aluri Srinivas,Goldman I. David

Funder

National Cancer Institute

Publisher

Elsevier BV

Subject

Clinical Biochemistry,Molecular Biology,Molecular Medicine,General Medicine,Biochemistry

Reference135 articles.

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4. Renal tubular reabsorption of folate mediated by folate binding protein 1;Birn;J. Am. Soc. Nephrol,2005

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