. . . . . . . . . . . . "[This produced an early-onset clinical syndrome that combines the severe phenotypes of SPG7 and SCA28, in additional to other 'mitochondrial' features such as oculomotor apraxia, extrapyramidal dysfunction, and myoclonic epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2015-02-27"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2015-08-25T14:46:20+02:00"^^ . . . . . . . . . . . "v3.0.0.0" . "v3.0.0" .