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Newman H, Perlman I, Pras E, Rozenberg A, Ben-Yosef T, Iovino C, Simonelli F, Di Iorio V, Rotenstreich Y, Katzburg E, Ehrenberg M, Iglicki M, Zur D. Newman H, et al. Among authors: ehrenberg m. Retina. 2022 Oct 1;42(10):e49. doi: 10.1097/IAE.0000000000003564. Retina. 2022. PMID: 36129272 No abstract available.
CRB1: one gene, many phenotypes.
Ehrenberg M, Pierce EA, Cox GF, Fulton AB. Ehrenberg M, et al. Semin Ophthalmol. 2013 Sep-Nov;28(5-6):397-405. doi: 10.3109/08820538.2013.825277. Semin Ophthalmol. 2013. PMID: 24138049 Review.
Retinal dystrophy as part of TTC21B-associated ciliopathy.
Ben-Yosef T, Asia Batsir N, Ali Nasser T, Ehrenberg M. Ben-Yosef T, et al. Among authors: ehrenberg m. Ophthalmic Genet. 2021 Jun;42(3):329-333. doi: 10.1080/13816810.2021.1888131. Epub 2021 Feb 18. Ophthalmic Genet. 2021. PMID: 33599192
A nationwide genetic analysis of inherited retinal diseases in Israel as assessed by the Israeli inherited retinal disease consortium (IIRDC).
Sharon D, Ben-Yosef T, Goldenberg-Cohen N, Pras E, Gradstein L, Soudry S, Mezer E, Zur D, Abbasi AH, Zeitz C, Cremers FPM, Khan MI, Levy J, Rotenstreich Y, Birk OS, Ehrenberg M, Leibu R, Newman H, Shomron N, Banin E, Perlman I. Sharon D, et al. Among authors: ehrenberg m. Hum Mutat. 2020 Jan;41(1):140-149. doi: 10.1002/humu.23903. Epub 2019 Sep 15. Hum Mutat. 2020. PMID: 31456290
282 results