Associated Papers
A novel GRHL2 nonsense variant impairs auditory function via a gain-of-function mechanism in autosomal dominant hearing loss.
Ma Y et al.
Acta Oto-laryngologica, 2026
Mutation screening in non-syndromic hearing loss patients with cochlear implantation by massive parallel sequencing in Taiwan.
Liu WH et al.
Plos One, 2019
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