Show pageBacklinksCite current pageExport to PDFBack to top This page is read only. You can view the source, but not change it. Ask your administrator if you think this is wrong. [[Neurofibromatosis type 2]] ([[NF2]]), a multiple [[neoplasia]] [[syndrome]], is a [[manifestation]] of an impaired [[expression]] of the [[merlin]] [[protein]], exerting [[inhibitor]]y effects on cell [[proliferation]] [[signal]]s due to abnormalities of the NF2 gene located on [[chromosome 22]]. About half of patients inherit a [[germline]] [[mutation]] from a parent, and nearly 60% of de novo NF2 patients are estimated to have somatic [[mosaicism]]. somatic_mosaicism.txt Last modified: 2024/06/07 03:00by 127.0.0.1