Mitochondrial calcium uniporter 2 deficiency

Type

Disease
External link(s)
- IEMbase
Gene
- MICU2 / Mitochondrial Calcium Uptake 2
  13q12.11
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Mitochondrial calcium uptake protein 2
Disease group(s)
- 11.1 Disorders of mitochondrial shuttles and carriers