. . . . . . . "[All mutations of atlastin1 in young-onset autosomal dominant spastic paraplegia patients in France were found in exons 7, 8, 12, and 13/exons should be given priority when performing molecular diagnoses for SPG3A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2009-03-31"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2017-10-17T13:18:29+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .