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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Published in | Acta ophthalmologica (Oxford, England) Vol. 93; no. S255 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Malden
Wiley Subscription Services, Inc
01.10.2015
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Subjects | |
Online Access | Get full text |
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