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) 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 <i>FLVCR1</i> gene. Ophthalmic Genetics. pp. 90-92. ISSN 1381-6810
(2020) Posterior column ataxia with retinitis pigmentosa (PCARP) in an Iranian patient associated with the FLVCR1 gene. Ophthalmic Genetics. pp. 90-92.