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    Novel co-occurrence of SLC26A4 and KCTD7 variants in a pediatric patient with syndromic hearing loss and myoclonic epilepsy

    Novel co-occurrence of SLC26A4 and KCTD7 variants in a pediatric patient with syndromic hearing loss and myoclonic epilepsy by Fakhreddin Shariatmadari, Amir Mahdi Mohamadi Kamal, Arshia Mobini, Shiva Bayat, Zahra Rezaei, Reza Shervin Badv, Mahmoud Mohammadi, Hossein Yousefimanesh

    Published 2025-06-01
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