Repository of Research and Investigative Information
Shahid Sadoughi University of Medical Sciences
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(2021) Apparent but unconfirmed digenism in an Iranian consanguineous family with syndromic Retinal Disease. Experimental Eye Research.
(2021) Autosomal Recessive Bestrophinopathy: Clinical and Genetic Characteristics of Twenty-Four Cases. Journal of Ophthalmology.
(2021) Homozygous females for a X-linked RPGR-ORF15 mutation in an Iranian family with retinitis pigmentosa. Experimental Eye Research.
(2020) Posterior column ataxia with retinitis pigmentosa (PCARP) in an Iranian patient associated with the FLVCR1 gene. Ophthalmic Genetics. pp. 90-92.
(2020) Slc30a8, cdkal1, tcf7l2, kcnq1 and igf2bp2 are associated with type 2 diabetes mellitus in iranian patients. Diabetes, Metabolic Syndrome and Obesity: Targets and Therapy. pp. 897-906.