. . . . . . . . . . . . "[CMT2A is an axonal autosomal dominant CMT type which in most cases is characterized by early onset and rather severe course.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2016-02-19"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2016-05-13T12:51:24+02:00"^^ . . . . . . . . . . . "v4.0.0.0" . "v4.0.0" .