. . . . . . . . . . . . "[MFN2 gene mutations were shown to be the most common cause of autosomal dominant hereditary axonopathy/addition, MFN2 gene mutations were also identified in CMT type 6 (axonal neuropathy with optic nerve atrophy).]. 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 . "2014-10-02T12:33:12+02:00"^^ . . . . . . . . . . . "v2.1.0.0" . "v2.1.0" .