BOLA3 deficiency

Synonym(s)
- Multiple mitochondrial dysfunctions syndrome type 2 with hyperglycinemia
Type

Disease
External link(s)
- Orphanet
- IEMbase
Gene
- BOLA3 / BolA Family Member 3
  2p13.1
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- BolA family member 3 protein
Disease group(s)
- 8.2 Disorders of lipoic acid and iron-sulfur metabolism