Associated Papers
Mechanistic insights into mutation in the proton-coupled folate transporter (SLC46A1) causing hereditary folate malabsorption.
Nandigrami P et al.
The Journal of Biological Chemistry, 2025
A proton-coupled folate transporter mutation causing hereditary folate malabsorption locks the protein in an inward-open conformation.
Zhan HQ et al.
The Journal of Biological Chemistry, 2020
A deep intronic mutation of c.1166-285 T > G in SLC46A1 is shared by four unrelated Japanese patients with hereditary folate malabsorption (HFM).
Tozawa Y et al.
Clinical Immunology (orlando, Fla.), 2019
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