Riboflavin transporter 3 deficiency

Synonym(s)
- Brown-Vialetto-van Laere syndrome type 1
Type

Disease
External link(s)
- Orphanet
- IEMbase
Gene
- SLC52A3 / Solute Carrier Family 52 Member 3
  20p13
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Riboflavin transporter 3
Disease group(s)
- 21.3 Disorders of riboflavin metabolism