A novel loss-of-function mutation in the proton-coupled folate transporter from a patient with hereditary folate malabsorption reveals that Arg 113 is crucial for function

I. Lasry, B. Berman, R. Straussberg, Y. Sofer, H. Bessler, M. Sharkia, F. Glaser, G. Jansen, S. Drori, Y.G. Assaraf

Research output: Contribution to journalArticleAcademicpeer-review

67 Citations (Scopus)
Original languageUndefined/Unknown
Pages (from-to)2055-2061
Issue number5
Publication statusPublished - 2008

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