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(2019) Novel splicing variant c. 208+2T > C in BBS5 segregates with Bardet-Biedl syndrome in an Iranian family by targeted exome sequencing. Bioscience Reports. p. 10. ISSN 0144-8463
(2018) Genetic identification and molecular modeling characterization reveal a novel PROM1 mutation in Stargardt4-like macular dystrophy. Oncotarget. pp. 122-141.
(2018) Identification of a novel RPGRIP1 mutation in an Iranian family with leber congenital amaurosis by exome sequencing. Journal of Cellular and Molecular Medicine. pp. 1733-1742. ISSN 1582-4934
(2018) In silico data analyses of the hotspot mutations of CHM gene in choroideremia disease. Data in Brief. pp. 1217-1223. ISSN 2352-3409 (Print) 2352-3409
(2018) Molecular genetics characterization and homology modeling of the CHM gene mutation: A study on its association with choroideremia. Mutat Res. pp. 39-50. ISSN 0027-5107