We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleNovel mutations in the KCNV2 gene in patients with cone dystrophy and a supernormal rod electroretinogram.AuthorsThiagalingam, Sureka; McGee, Terri L; Weleber, Richard G; Sandberg, Michael A; Trzupek, Karmen M; Berson, Eliot L; Dryja, Thaddeus PAbstractTo identify mutations in KCNV2 in patients with a form of cone dystrophy characterized by a supernormal rod electroretinogram (ERG).PublicationOphthalmic genetics, 2007, Vol 28, Issue 3, p135ISSN1381-6810Publication typeJournal ArticleDOI10.1080/13816810701503681