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Genetic spectrum of retinal dystrophies in Tunisia.
Habibi I, Falfoul Y, Turki A, Hassairi A, El Matri K, Chebil A, Schorderet DF, El Matri L. Habibi I, et al. Among authors: schorderet df. Sci Rep. 2020 Jul 8;10(1):11199. doi: 10.1038/s41598-020-67792-y. Sci Rep. 2020. PMID: 32641690 Free PMC article.
Identifying mutations in Tunisian families with retinal dystrophy.
Habibi I, Chebil A, Falfoul Y, Allaman-Pillet N, Kort F, Schorderet DF, El Matri L. Habibi I, et al. Among authors: schorderet df. Sci Rep. 2016 Nov 22;6:37455. doi: 10.1038/srep37455. Sci Rep. 2016. PMID: 27874104 Free PMC article.
[No title available]
[No authors listed] [No authors listed] PMID: 31748608
Clinical and Genetic Findings of Autosomal Recessive Bestrophinopathy (ARB).
Habibi I, Falfoul Y, Todorova MG, Wyrsch S, Vaclavik V, Helfenstein M, Turki A, Matri KE, Matri LE, Schorderet DF. Habibi I, et al. Among authors: schorderet df. Genes (Basel). 2019 Nov 21;10(12):953. doi: 10.3390/genes10120953. Genes (Basel). 2019. PMID: 31766397 Free PMC article.
Different Phenotypes in Pseudodominant Inherited Retinal Dystrophies.
Habibi I, Falfoul Y, Tran HV, El Matri K, Chebil A, El Matri L, Schorderet DF. Habibi I, et al. Among authors: schorderet df. Front Cell Dev Biol. 2021 Feb 5;9:625560. doi: 10.3389/fcell.2021.625560. eCollection 2021. Front Cell Dev Biol. 2021. PMID: 33634125 Free PMC article.
Phenotype of three consanguineous Tunisian families with early-onset retinal degeneration caused by an R91W homozygous mutation in the RPE65 gene.
El Matri L, Ambresin A, Schorderet DF, Kawasaki A, Seeliger MW, Wenzel A, Arsenijevic Y, Borruat FX, Munier FL. El Matri L, et al. Among authors: schorderet df. Graefes Arch Clin Exp Ophthalmol. 2006 Sep;244(9):1104-12. doi: 10.1007/s00417-005-0096-2. Epub 2006 Feb 28. Graefes Arch Clin Exp Ophthalmol. 2006. PMID: 16518657
285 results