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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

About the Authors

Giulia Venturini, Carlo Rivolta
Department of Medical Genetics, University of Lausanne, Lausanne, Switzerland
Anna M. Rose, Amna Z. Shah, Shomi S. Bhattacharya
Department of Genetics, UCL Institute of Ophthalmology, University College London, London, United Kingdom

Corresponding Author

Email: carlo.rivolta@unil.ch

Competing Interests

The authors have declared that no competing interests exist.

Author Contributions

Conceived and designed the experiments: GV SSB CR. Performed the experiments: GV AMR AZS CR. Analyzed the data: GV CR. Contributed reagents/materials/analysis tools: AMR AZS SSB. Wrote the paper: GV CR.