Spartin deficiency

Type

Disease
External link(s)
- IEMbase
Gene
- SPG20 / Spartin
  13q12.3
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Spartin
Disease group(s)
- 19.2 Disorders of mitochondrial and peroxisomal dynamics