TIMM22 deficiency

Type

Disease
External link(s)
- IEMbase
Gene
- TIMM22 / Translocase of Inner Mitochondrial Membrane 22
  17p13
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Mitochondrial import inner membrane translocase subunit TIM22
Disease group(s)
- 11.2 Disorders of mitochondrial protein import