Back to matchesWe found a matchYour institution may have rights to this item. Sign in to continue.TitleIdentification of a founder mutation in KRT14 associated with Naegeli–Franceschetti–Jadassohn syndrome.AuthorsRalser, D.J.; Kumar, S.; Borisov, O.; Sarig, O.; Richard, G.; Wolf, S.; Krawitz, P.M.; Sprecher, E.; Kreiß, M.; Betz, R.C.SubjectsSYNDROMES; PALMOPLANTAR keratoderma; GENETIC drift; ECTODERMAL dysplasia; GENETIC mutation; DNA analysis; EPIDERMOLYSIS bullosaPublicationBritish Journal of Dermatology, 2020, Vol 183, Issue 4, p756ISSN0007-0963Publication typeArticleDOI10.1111/bjd.19123