Associated Papers
Identification of two novel mutations in POU4F3 gene associated with autosomal dominant hearing loss in Chinese families.
Bai X et al.
Journal of Cellular and Molecular Medicine, 2020
Exome sequencing identifies POU4F3 as the causative gene for a large Chinese family with non-syndromic hearing loss.
Cai XZ et al.
Journal of Human Genetics, 2017
POU4F3 mutation screening in Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis identified novel variants associated with autosomal dominant hearing loss.
Kitano T et al.
Plos One, 2017
A novel frameshift mutation of POU4F3 gene associated with autosomal dominant non-syndromic hearing loss.
Lee HK et al.
Biochemical and Biophysical Research Communications, 2010
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