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      Prevalence of disease-causing mutations in families with autosomal dominant retinitis pigmentosa: a screen of known genes in 200 families.

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          Abstract

          To survey families with clinical evidence of autosomal dominant retinitis pigmentosa (adRP) for mutations in genes known to cause adRP.

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          Author and article information

          Journal
          Invest Ophthalmol Vis Sci
          Investigative ophthalmology & visual science
          Association for Research in Vision and Ophthalmology (ARVO)
          0146-0404
          0146-0404
          Jul 2006
          : 47
          : 7
          Affiliations
          [1 ] Human Genetics Center, School of Public Health, Department of Ophthalmology and Visual Science, the University of Texas Health Science Center, Houston 77030, USA. lori.s.sullivan@uth.tmc.edu
          Article
          47/7/3052 NIHMS76443
          10.1167/iovs.05-1443
          2585061
          16799052
          47b8bc07-cd2e-4248-bff3-6c4e3a42566a
          History

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