Abstract 4134 Mechanistic insights into mutations in the human proton-coupled folate transporter (SLC46A1) causing hereditary folate malabsorption
P
Prithviraj Nandigrami
I
I. David Goldman
A
Andras Fiser
Article Details
Journal
Journal of Biological Chemistry
Volume / Issue
Vol. 302, Issue 5
Published
May 01, 2026
Pages
112816
ISSN
0021-9258
Publisher
Elsevier BV
Authors (3)
P
Prithviraj Nandigrami
I
I. David Goldman
A
Andras Fiser
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