. . . . . . . . . . . . "[In conclusion, we confirm that EGR2 mutations are not frequent in HMSN and represent <1% of the cases. Their occurrence seems restricted to the more severe phenotypes of DSS and CH but they are also, more rarely, associated with a CMT1 phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2015-02-21"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2015-08-25T14:38:09+02:00"^^ . . . . . . . . . . . "v3.0.0.0" . "v3.0.0" .