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Dominant and recessive ATOH1 variants cause distinct neurodevelopmental disorders with hearing loss

Nicole Bertola et al.
HAL (France) · Papers · License: Open Access
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hearing-lossneurodevelopmental-disorder
Protein turnover, Mechanosensory hair cells, Hearing loss, 0, ATOH1, Hindbrain malformation, Transcription factor, Neurodevelopmental disorder
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Record · ID 308244
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