combined oxidative phosphorylation deficiency 11 (Q102297041)
Jump to navigation
Jump to search
human disease
- COXPD11
- infantile encephaloneuromyopathy due to mitochondrial translation defect
- Combined oxidative phosphorylation defect type 11
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | combined oxidative phosphorylation deficiency 11 |
human disease |
|
Statements
1 reference
1 reference
Identifiers
1 reference