RS775046032 TWNK
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Associated Conditions
Infantile onset spinocerebellar ataxia
Perrault syndrome 5
Progressive external ophthalmoplegia with mitochondrial DNA deletions
autosomal dominant 3
Infantile onset spinocerebellar ataxia
Perrault syndrome 5
Progressive external ophthalmoplegia with mitochondrial DNA deletions
autosomal dominant 3
Other Variants in TWNK