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Research Article

CNOT3 Is a Modifier of PRPF31 Mutations in Retinitis Pigmentosa with Incomplete Penetrance

  • Giulia Venturini,

    Affiliation: Department of Medical Genetics, University of Lausanne, Lausanne, Switzerland

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  • Anna M. Rose,

    Affiliation: Department of Genetics, UCL Institute of Ophthalmology, University College London, London, United Kingdom

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  • Amna Z. Shah,

    Affiliation: Department of Genetics, UCL Institute of Ophthalmology, University College London, London, United Kingdom

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  • Shomi S. Bhattacharya,

    Affiliation: Department of Genetics, UCL Institute of Ophthalmology, University College London, London, United Kingdom

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  • Carlo Rivolta mail

    carlo.rivolta@unil.ch

    Affiliation: Department of Medical Genetics, University of Lausanne, Lausanne, Switzerland

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  • Published: November 08, 2012
  • DOI: 10.1371/journal.pgen.1003040

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