Back to matchesWe found a matchYour institution may have rights to this item. Sign in to continue.TitleNovel VPS33B mutation in a patient with autosomal recessive keratoderma‐ichthyosis‐deafness syndrome.AuthorsAlter, Svenja; Hotz, Alrun; Jahn, Arne; Di Donato, Nataliya; Schröck, Evelin; Smitka, Martin; von der Hagen, Maja; Schallner, Jens; Menschikowski, Mario; Gillitzer, Claus; Laass, Martin W.; Fischer, Judith; Tzschach, AndreasPublicationAmerican Journal of Medical Genetics. Part A, 2018, Vol 176, Issue 12, p2862ISSN1552-4825Publication typeArticleDOI10.1002/ajmg.a.40634