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 S; McGee TL; Weleber RG; Sandberg MA; Trzupek KM; Berson EL; Dryja TPPublicationOphthalmic genetics, 2007, Vol 28, Issue 3, p135ISSN1381-6810Publication typearticleDOI10.1080/13816810701503681