We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleClinical characterization, linkage analysis, and PRPC8 mutation analysis of a family with autosomal dominant retinitis pigmentosa type 13 (RP13).Authorsvan Lith-Verhoeven JJ; van der Velde-Visser SD; Sohocki MM; Deutman AF; Brink HM; Cremers FP; Hoyng CBPublicationOphthalmic genetics, 2002, Vol 23, Issue 1, p1ISSN1381-6810Publication typearticleDOI10.1076/opge.23.1.1.2206