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Cited by in F6Publishing
For: Mairot K, Smirnov V, Bocquet B, Labesse G, Arndt C, Defoort-Dhellemmes S, Zanlonghi X, Hamroun D, Denis D, Picot MC, David T, Grunewald O, Pégart M, Huguet H, Roux AF, Kalatzis V, Dhaenens CM, Meunier I. CRB1-Related Retinal Dystrophies in a Cohort of 50 Patients: A Reappraisal in the Light of Specific Müller Cell and Photoreceptor CRB1 Isoforms. Int J Mol Sci 2021;22:12642. [PMID: 34884448 DOI: 10.3390/ijms222312642] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
Number Citing Articles
1 Daich Varela M, Georgiou M, Alswaiti Y, Kabbani J, Fujinami K, Fujinami-Yokokawa Y, Khoda S, Mahroo OA, Robson AG, Webster AR, AlTalbishi A, Michaelides M. CRB1-Associated Retinal Dystrophies: Genetics, Clinical Characteristics, and Natural History. Am J Ophthalmol 2023;246:107-21. [PMID: 36099972 DOI: 10.1016/j.ajo.2022.09.002] [Reference Citation Analysis]
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3 Santos DF, Molina Thurin LJ, Vargas JG, Izquierdo NJ, Oliver A. Retinitis Pigmentosa in the Puerto Rican Population: A Geographic Distribution. OPTH 2022;Volume 16:3175-3179. [DOI: 10.2147/opth.s375365] [Reference Citation Analysis]
4 Bhardwaj A, Yadav A, Yadav M, Tanwar M. Genetic dissection of non-syndromic retinitis pigmentosa. Indian J Ophthalmol 2022;70:2355-85. [PMID: 35791117 DOI: 10.4103/ijo.IJO_46_22] [Reference Citation Analysis]
5 Sun J, Yan H, Hu D, Zhou J, Wang Y, Wu J, Song X, Hou X. Biallelic Heterozygous Mutations in Crumbs Homolog-1 Gene Associated With Macular Retinoschisis and Angle-Closure Glaucoma: A Case Report and Literature Review. Front Ophthalmol 2022;2. [DOI: 10.3389/fopht.2022.902898] [Reference Citation Analysis]