Rehman, Atta UrSepahi, NedaBedoni, NicolaRavesh, ZeinabSalmaninejad, ArashCancellieri, FrancescaPeter, Virginie G.Quinodoz, MathieuMojarrad, MajidPasdar, AlirezaAsad, Ali GhanbariGhalamkari, SamanPiran, MehranPiran, MehrdadSuperti-Furga, AndreaRivolta, Carlo2021-11-022021-11-022021-12-01Rehman, A U, Sepahi, N, Bedoni, N, Ravesh, Z, Salmaninejad, A, Cancellieri, F, Peter, V G, Quinodoz, M, Mojarrad, M, Pasdar, A, Asad, A G, Ghalamkari, S, Piran, M, Piran, M, Superti-Furga, A & Rivolta, C 2021, 'Whole exome sequencing in 17 consanguineous Iranian pedigrees expands the mutational spectrum of inherited retinal dystrophies', Scientific Reports, vol. 11, no. 1, 19332. https://doi.org/10.1038/s41598-021-98677-32045-2322ORCID: /0000-0002-7864-9729/work/102536735https://hdl.handle.net/2164/17431Funding Information: We would like to thank all of the participating families. We are also grateful to the Swiss Confederation for the award of a PhD fellowship to AUR, to Mashhad University of Medical Sciences for supporting part of the work, in the framework of the PhD thesis of AS, to the Swiss National Science Foundation for grant # 176097 to CR, and to the Fondation Guillaume Gentil for support to ASF.91068853engSDG 3 - Good Health and Well-beingR Medicine (General)GeneralOtherR1Journal article10.1038/s41598-021-98677-3http://www.scopus.com/inward/record.url?scp=85116346473&partnerID=8YFLogxK111