. "An autosomal dominant cerebellar ataxia that is characterized by progressive ataxia, dysarthria, hyperreflexia, ophthalmoparesis, nystagmus and ptosis, and has_material_basis_in mutation in the AFG3L2 gene."^^ . . "spinocerebellar ataxia type 28"^^ . "2015-10-06T16:11:07Z"^^ . _:vb50938005 . _:vb50938005 . . "DOID:0050977"^^ . "lschriml"^^ . _:vb50938005 . _:vb50938005 . "disease_ontology"^^ . _:vb50938005 . "OMIM:610246"^^ .