. . . . . . . . . . . . "[7 new SPG4 point mutations (including missense mutations R364T, L380H, M579H) and 2 new deletions are reported/mutations and deletions are a significant cause of hereditary spastic paraplegia.]. 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 . "2014-10-02T12:33:14+02:00"^^ . . . . . . . . . . . "v2.1.0.0" . "v2.1.0" .