tRNA 5-taurinomethyluridine modifier deficiency

Synonym(s)
- Combined oxidative phosphorylation deficiency type 23
Type

Disease
External link(s)
- Orphanet
- IEMbase
Gene
- GTPBP3 / Mitochondrial GTP Binding Protein 3
  19p13.11
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Mitochondrial GTP-binding protein 3
Disease group(s)
- 10.1 Disorders of mitochondrial transcript processing and modification