Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleIdentification of p.A684V missense mutation in the WFS1 gene as a frequent cause of autosomal dominant optic atrophy and hearing impairment.AuthorsRendtorff, Nanna D.; Lodahl, Marianne; Boulahbel, Houda; Johansen, Ida R.; Pandya, Arti; Welch, Katherine O.; Norris, Virginia W.; Arnos, Kathleen S.; Bitner-Glindzicz, Maria; Emery, Sarah B.; Mets, Marilyn B.; Fagerheim, Toril; Eriksson, Kristina; Hansen, Lars; Bruhn, Helene; Möller, Claes; Lindholm, Sture; Ensgaard, Stefan; Lesperance, Marci M.; Tranebjaerg, LisbethPublicationAmerican Journal of Medical Genetics. Part A, 2011, Vol 155A, Issue 6, p1298ISSN1552-4825Publication typeArticleDOI10.1002/ajmg.a.33970