Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleMutation in the PYK2-binding domain of PITPNM3 causes autosomal dominant cone dystrophy (CORD5) in two Swedish families.AuthorsKöhn L; Kadzhaev K; Burstedt MS; Haraldsson S; Hallberg B; Sandgren O; Golovleva IPublicationEuropean journal of human genetics : EJHG, 2007, Vol 15, Issue 6, p664ISSN1018-4813Publication typearticleDOI10.1038/sj.ejhg.5201817