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Whole exome sequencing in 17 consanguineous Iranian pedigrees expands the mutational spectrum of inherited retinal dystrophies
Atta Ur Rehman, Neda Sepahi, Nicola Bedoni, Zeinab Ravesh, Arash Salmaninejad, Francesca Cancellieri, Virginie G. Peter, Mathieu Quinodoz, Majid Mojarrad, Alireza Pasdar, Ali Ghanbari Asad, Saman Ghalamkari, Mehran Piran, Mehrdad Piran, Andrea Superti-Furga, Carlo Rivolta*
*Corresponding author for this work
- University of Lausanne
- Fasa University of Medical Sciences
- University of Leicester
- Mashhad University of Medical Sciences
- Institute of Molecular and Clinical Ophthalmology Basel (IOB)
- University of Basel
- Department of Medical Genetics and Molecular Medicine
- University of Aberdeen
- Persian Bayangene Research and Training Institute
Research output: Contribution to journal › Article › peer-review
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