. . . . . . . . . . . . "[The spectrum of clinical phenotype caused by MeCP2 mutations is wide, including milder preserved speech variants, the severe congenital Rett variant, and a subset of X-linked recessive mental retardation in boys.]. 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 . "2016-05-13T12:44:28+02:00"^^ . . . . . . . . . . . "v4.0.0.0" . "v4.0.0" .