Rubicon deficiency

Synonym(s)
- Autosomal recessive spinocerebellar ataxia type 15
Type

Disease
External link(s)
- Orphanet
- IEMbase
Gene
- RUBCN / Rubicon, autophagy regulator
  3q29
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Rubicon
Disease group(s)
- 19.6.4 Other disorders of vesicular trafficking