Associated Papers
Next-Generation Sequencing Identifies Pathogenic Variants in HGF, POU3F4, TECTA, and MYO7A in Consanguineous Pakistani Deaf Families.
Mei X et al.
Neural Plasticity, 2021
De novo mutation in X-linked hearing loss-associated POU3F4 in a sporadic case of congenital hearing loss.
Moteki H et al.
The Annals of Otology, Rhinology, and Laryngology, 2015
Cochlear implantation in children with congenital X-linked deafness due to novel mutations in POU3F4 gene.
Stankovic KM et al.
The Annals of Otology, Rhinology, and Laryngology, 2010
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