Showing 1 - 2 results of 2 for search 'Nahid Rezaie', query time: 0.01s Refine Results
  1. 1
    A novel frameshift variant in the TMPRSS3 gene causes nonsyndromic hearing loss in a consanguineous family

    A novel frameshift variant in the TMPRSS3 gene causes nonsyndromic hearing loss in a consanguineous family by Nahid Rezaie, Saeedeh Sadat Ghazanfari, Seyede Mahsa Mousavikia, Nader Mansour Samaei, Morteza Oladnabi, Abdolazim Sarli, Teymoor Khosravi

    Published 2024-11-01
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  2. 2
    CCDC82 and neurodevelopment: a novel genetic variant linked to infantile spasms and hypotonia

    CCDC82 and neurodevelopment: a novel genetic variant linked to infantile spasms and hypotonia by Zahra Safarian, Shiva Mehrabi, Arghavan Rakhshani Nejad, Sajad Alavimanesh, Pegah Kavousinia, Mohammad Hossein Shushizadeh, Seyedeh Faezeh Hassani, Latifeh Onagh, Abdolazim Sarli, Nahid Rezaie

    Published 2025-08-01
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