Original language | Undefined/Unknown |
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Pages (from-to) | 2055-2061 |
Journal | Blood |
Volume | 112 |
Issue number | 5 |
DOIs | |
Publication status | Published - 2008 |
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 journal › Article › Academic › peer-review