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2017

2017-Present: “Genetic Profiling of Common Hereditary Disorders to Identify the Distribution of Mutations in Iran Provinces: Hope Project”

Principal Investigator: SR Ghaffari Principal associate Investigator: M Rafati The first phase of this project which attracted >700,000$ has focused on genetic profiling of 1000 patients (in the first phase) with inborn errors of metabolism, neurogenetic disorders or inherited retinal dystrophies by targeted capture sequencing […]

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2007

2007-2011: Determining the Distribution of Different Modes of Inheritance among Iranian Patients with Retinitis Pigmentosa by Pedigree Analysis of ~14000 Iranian RP patients from >4000 Families registered in Iran RP Society

Principal Investigator: SR Ghaffari Principal associate Investigator: M Rafati Other Investigators: N Novin, S Khorrami, Following starting collaboration with Iran RP Society, the database of RP patients was redesigned to add new data about genetic aspects of […]