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

Open Access

Peer-reviewed

Research Article

Giulia Venturini,

Affiliation Department of Medical Genetics, University of Lausanne, Lausanne, Switzerland
⨯
Anna M. Rose,

Affiliation Department of Genetics, UCL Institute of Ophthalmology, University College London, London, United Kingdom
⨯
Amna Z. Shah,

Affiliation Department of Genetics, UCL Institute of Ophthalmology, University College London, London, United Kingdom
⨯
Shomi S. Bhattacharya,

Affiliation Department of Genetics, UCL Institute of Ophthalmology, University College London, London, United Kingdom
⨯
Carlo Rivolta

* E-mail: carlo.rivolta@unil.ch

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

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Mutation
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Heredity
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Small interfering RNA
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Gene expression
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Immunoprecipitation
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Polymerase chain reaction
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Retinitis pigmentosa
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Chromosome mapping
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