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      Phenotype of Retinitis Pigmentosa Associated With the Ser50Thr Mutation in the NRL Gene

      Archives of Ophthalmology

      American Medical Association (AMA)

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          Abstract

          <p class="first" id="d6314341e83">We previously reported an Ser50Thr mutation in the NRL gene as a cause of autosomal dominant retinitis pigmentosa. </p>

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          Author and article information

          Journal
          Archives of Ophthalmology
          Arch Ophthalmol
          American Medical Association (AMA)
          0003-9950
          June 01 2003
          June 01 2003
          : 121
          : 6
          : 793
          Article
          10.1001/archopht.121.6.793
          12796249
          © 2003

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