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folate malabsorption, congenital
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Journal Articles

Hereditary folate malabsorption due to a mutation in the external gate of the proton-coupled folate transporter SLC46A1

Srinivas Aluri, Rongbao Zhao, Charlotte Lubout, Susanna M. I. Goorden, Andras Fiser, I. David Goldman
Journal: Blood Advances
Blood Adv (2018) 2 (1): 61–68.
https://doi.org/10.1182/bloodadvances.2017012690
Published: 2018