Hasil Pencarian - Kamila Hanková

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    A TBC1D24 gene variant coincides with STRC compound heterozygosity in a family with hearing loss: a case report

    A TBC1D24 gene variant coincides with STRC compound heterozygosity in a family with hearing loss: a case report oleh Martin Schwarz, Kamila Hanková, Markéta Havlovicová, Radka Kremlíková Pourová, Jan Bouček

    Diterbitkan 2024-10-01
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