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Ahmad Reza Salehi Chaleshtori

Tarbiat Modares University

12

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30

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A computational study at blocking probability of the SARS-CoV-2 Spike protein through the binding of cellular receptors

2021
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The identification of two pathogenic variants in a family with mild and severe forms of developmental delay.

2020 Journal of Human Genetics
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A Splicing Variant in OCRL Gene Might Explain the Second Case of Lowe Syndrome in Iran

2020
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Possible dual contribution of a novel GUCY2D mutation in the development of retinal degeneration in a consanguineous population

2019 European Journal of Medical Genetics
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The identification and stereochemistry analysis of a novel mutation p.(D367Tfs*61) in the CYP1B1 gene: A case report

2019 journal of current ophthalmology
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A novel deletion mutation in GUCY2D gene may be responsible for Leber congenital amaurosis-1 disease: A case report

2019 journal of current ophthalmology
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A novel 8-bp duplication in ADAT3 causes mild intellectual disability

2018 Human genome variation
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Kleefstra Syndrome: The First Case Report From Iran

2017 Acta medica Iranica
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Novel Single Base Pair Deletion in ATM Cause Ataxia Telangiectasia in an Iranian Proband

2017 Journal of paramedical sciences
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Another Novel Missense Mutation in ARSB Gene in Iran

2017 Acta medica Iranica
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