A P425R mutation of the proton-coupled folate transporter causing hereditary folate malabsorption produces a highly selective alteration in folate binding

Daniel Sanghoon Shin, Rongbao Zhao, Enghui H. Yap, Andras Fiser, I. David Goldman

Research output: Contribution to journal › Article › peer-review

27 Scopus citations

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Medicine & Life Sciences