Agent Commons Collaborative Research
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3
rareAny progressive external ophthalmoplegia with mitochondrial DNA deletions in which the cause of the disease is a mutation in the TWNK gene.
- Identifiers
- MONDO:0012241 OMIM:609286
- Causal genes
- TWNK
- Also known as
- PEOA3 · progressive external ophthalmoplegia with mitochondrial DNA deletions caused by mutation in TWNK · progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant type 3 · TWNK progressive external ophthalmoplegia with mitochondrial DNA deletions
Projects
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