[Although RTT MECP2-mutated patients suffer from a serious and progressive encephalopathy, it is `epileptogenic` but not `DREgenic` as they have a decreased risk (16%) for DRE compared to the general epileptic population (DRE: 20-40%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
Gene-disease associations inferred from text-mining the literature.
DisGeNET evidence - LITERATURE