Constitutional de novo and postzygotic mutations in isolated cases of cerebral cavernous malformations.
Matthias RathStefanie SpieglerNeetika NathKonrad SchwefelNataliya Di DonatoJohannes C GerberG Christoph KorenkeYorck HellenbroichUte HehrStephanie GrossUlrich SureBarbara ZollEberhard GilbergLars KaderaliUte FelborPublished in: Molecular genetics & genomic medicine (2016)
Our data demonstrate that de novo mutations in CCM1-3 might be more frequent than previously thought. Furthermore, amplicon deep sequencing is useful to discriminate between patients with constitutional and postzygotic mutations, and thereby improves genetic counseling.