. . . . . . . "[Our data broaden the phenotype of IBMPFD to include motor neuron degeneration, suggest that VCP mutations may account for ?1%-2% of familial ALS, and provide evidence directly implicating defects in the ubiquitination/protein degradation pathway in motor neuron degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2017-02-19"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2017-10-17T13:17:11+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .