Salmaninejad, ArashBedoni, NicolaRavesh, ZeinabQuinodoz, MathieuShoeibi, NasserMojarrad, MajidPasdar, AlirezaRivolta, Carlo2021-01-252021-01-252020-11-10Salmaninejad, A, Bedoni, N, Ravesh, Z, Quinodoz, M, Shoeibi, N, Mojarrad, M, Pasdar, A & Rivolta, C 2020, 'Whole exome sequencing and homozygosity mapping reveals genetic defects in consanguineous Iranian families with inherited retinal dystrophies', Scientific Reports, vol. 10, 19413. https://doi.org/10.1038/s41598-020-75841-92045-2322ORCID: /0000-0002-7864-9729/work/88320239https://hdl.handle.net/2164/15720Acknowledgements This research was funded by the Swiss National Science Foundation (Grant #176097 to CR). We would like to express gratitude to the patients and all their family members that participated in this study for their valuable cooperation and participation.72037826engGenetic variationGeneticsgenomemedical geneticsMutationR MedicineSupplementary DataRJournal article10.1038/s41598-020-75841-9http://www.scopus.com/inward/record.url?scp=85095722074&partnerID=8YFLogxK10