Brown-Vialetto-van Laere syndrome 1

Any Brown-Vialetto-van Laere syndrome in which the cause of the disease is a mutation in the SLC52A3 gene.

Also known as: Brown-Vialetto-Van Laere syndrome 1, Brown-Vialetto-van Laere syndrome 1, Brown-Vialetto-van Laere syndrome caused by mutation in SLC52A3, RTD2, Riboflavin transporter deficiency 2, SLC52A3 Brown-Vialetto-van Laere syndrome, rfvt2-related riboflavin transporter deficiency, BVVLS1

10 clinical trials for this condition and its sub-types, 0 tagged with Brown-Vialetto-van Laere syndrome 1 itself.