Literature associating SLC52A1 and lateral medullary syndrome
SLC52A1 [ENSP00000399979]
Solute carrier family 52, riboflavin transporter, member 1; Plasma membrane transporter mediating the uptake by cells of the water soluble vitamin B2/riboflavin that plays a key role in biochemical oxidation-reduction reactions of the carbohydrate, lipid, and amino acid metabolism . Humans are unable to synthesize vitamin B2/riboflavin and must obtain it via intestinal absorption .
Synonyms: SLC52A1, SLC52A1p, hSLC52A1, F5H5Y1, Q9NWF4 ...