Exome sequencing confirms ZNF408 mutations as a cause of familial retinitis pigmentosa

Purpose The aim of this study was to identify the gene causing retinitis pigmentosa (RP) in a Tunisian family. Methods Three members of a consanguineous Tunisian family were clinically examined and were given best‐corrected visual acuity (BCVA), slit lamp biomicroscopy, fundus photography and optica...

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Bibliographic Details
Published inActa ophthalmologica (Oxford, England) Vol. 93; no. S255
Main Authors Habibi, I., Chebil, A., Kort, F., Munier, F., Schorderet, D., El Matri, L.
Format Journal Article
LanguageEnglish
Published Malden Wiley Subscription Services, Inc 01.10.2015
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