Barashkov, Nikolay A.; Romanov, Georgii P.; Borisova, Uigulaana P.; Solovyev, Aisen V.; Pshennikova, Vera G.; Teryutin, Fedor M.; Bondar, Alexander A.; Morozov, Igor V.; Khusnutdinova, Elza K.; Posukh, Olga L.; Burtseva, Tatiana E.; Odland, Jon Øyvind; Fedorova, Sardana A. (Peer reviewed; Journal article, 2019)
Waardenburg syndrome (WS) is an orphan genetic disease with autosomal dominant pattern of inheritance characterised by varying degrees of hearing loss accompanied by skin, hair and iris pigmentation abnormalities. Four ...