We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleDeleterious mutation in GPSM2 identified as cause for nonsyndromic deafness.AuthorsSchulze, JmPublicationClinical genetics, 2011, Vol 79, Issue 1, p44ISSN1399-0004Publication typeJournal ArticleDOI10.1111/j.1399-0004.2010.01556_1.x