Search Results - Sima Rayat

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    Novel homozygous variants in the TMC1 and CDH23 genes cause autosomal recessive nonsyndromic hearing loss by Safoura Zardadi, Ehsan Razmara, Golareh Asgaritarghi, Ehsan Jafarinia, Fatemeh Bitarafan, Sima Rayat, Navid Almadani, Saeid Morovvati, Masoud Garshasbi

    Published in Molecular Genetics & Genomic Medicine (2020-12-01)
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  2. 2

    The clinical and genetic spectrum of twenty-six individuals with hearing loss affected by MYO15A variants by Saeid Morovvati, Mina Mohammadi Sarband, Samaneh Doostmohammadi, Sima Rayat, Hessamaldin Emamdjomeh, Mohammad Farhadi, Alimohamad Asghari, Masoud Garshasbi, Masoumeh Falah

    Published in Scientific Reports (2025-04-01)
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