QuickView for Cox20p (gene)

No studies found

1. Clinical and genetic characteristics of children with COX20-associated mitochondrial disorder: case …
2. Bi-allelic loss of function variants in COX20 gene cause autosomal recessive sensory neuronopathy.
3. The lncRNA DANCR promotes development of atherosclerosis by regulating the miR-214-5p/COX20 signalin…
4. The phenotypic spectrum of COX20-associated mitochondrial disorder.
5. The mitochondrial TMEM177 associates with COX20 during COX2 biogenesis.

There were no clinical trials for Cox20p