Search Results - Saeid Morovvati

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  1. 1
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    CAD gene and early infantile epileptic encephalopathy-50; three Iranian deceased patients and a novel mutation: case report by Sepideh Gholami Yarahmadi, Saeid Morovvati

    Published 2022
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  2. 2
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    Analysis of TMIE gene mutations including the first large deletion of exon 1 with autosomal recessive non-syndromic deafness by Sima Rayat, Mohammad Farhadi, Hessamaldin Emamdjomeh, Saeid Morovvati, Masoumeh Falah

    Published 2022
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    Waardenburg syndrome type 2A in a large Iranian family with a novel MITF gene mutation by Safoura Zardadi, Sima Rayat, Maryam Hassani Doabsari, Mohammad Keramatipour, Saeid Morovvati

    Published 2021
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    Four mutations in MITF, SOX10 and PAX3 genes were identified as genetic causes of waardenburg syndrome in four unrelated Iranian patients: case report by Safoura Zardadi, Sima Rayat, Maryam Hassani Doabsari, Aliagha Alishiri, Mohammad Keramatipour, Zeynab Javanfekr Shahri, Saeid Morovvati

    Published 2021
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