Back to matchesWe found a matchYour institution may have rights to this item. Sign in to continue.TitleMutations in PLS1, encoding fimbrin, cause autosomal dominant nonsyndromic hearing loss.AuthorsMorgan, Anna; Koboldt, Daniel C.; Barrie, Elizabeth S.; Crist, Erin R.; García García, Gema; Mezzavilla, Massimo; Faletra, Flavio; Mihalic Mosher, Theresa; Wilson, Richard K.; Blanchet, Catherine; Manickam, Kandamurugu; Roux, Anne‐Francoise; Gasparini, Paolo; Dell'Orco, Daniele; Girotto, GiorgiaPublicationHuman Mutation, 2019, Vol 40, Issue 12, p2286ISSN1059-7794Publication typeArticleDOI10.1002/humu.23891