Whole exome sequencing in 17 consanguineous Iranian pedigrees expands the mutational spectrum of inherited retinal dystrophies.
Rehman AU, Sepahi N, Bedoni N, Ravesh Z, Salmaninejad A, Cancellieri F, Peter VG, Quinodoz M, Mojarrad M, Pasdar A, Asad AG, Ghalamkari S, Piran M, Piran M, Superti-Furga A, Rivolta C.
Rehman AU, et al. Among authors: ghalamkari s.
Sci Rep. 2021 Sep 29;11(1):19332. doi: 10.1038/s41598-021-98677-3.
Sci Rep. 2021.
PMID: 34588515
Free PMC article.