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[2] SLC52A2 [p.P141T] and SLC52A3 [p.N21S] causing Brown-Vialetto-Van Laere Syndrome in an Indian patient: First genetically proven case with mutations in two riboflavin transporters.Clin Chim Acta. 2016 Nov 1;462:210-214.

[3] SLC52A3 expression is activated by NF-kappaB p65/Rel-B and serves as a prognostic biomarker in esophageal cancer.Cell Mol Life Sci. 2018 Jul;75(14):2643-2661.