Identification of a founder mutation in KRT14 associated with Naegeli–Franceschetti–Jadassohn syndrome. (1st October 2020) - Ralser, D.J.; Kumar, S.; Borisov, O.; Sarig, O.; Richard, G.; Wolf, S.; Krawitz, P.M.; Sprecher, E.; Kreiß, M.; Betz, R.C.