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Dive into the research topics of 'Hereditary folate malabsorption due to a mutation in the external gate of the proton-coupled folate transporter SLC46A1'. Together they form a unique fingerprint.- Sort by
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Srinivas Aluri, Rongbao Zhao, Charlotte Lubout, Susanna M.I. Goorden, Andras Fiser, I. David Goldman
Research output: Contribution to journal › Article › peer-review