Associated Papers
A New Pathogenic Variant in POU3F4 Causing Deafness Due to an Incomplete Partition of the Cochlea Paved the Way for Innovative Surgery.
Tekin AM et al.
Genes, 2021
Clinical and molecular characterization of POU3F4 mutations in multiple DFNX2 Chinese families.
Su Y et al.
Bmc Medical Genetics, 2018
A novel mutation in POU3F4 in a Chinese family with X-linked non-syndromic hearing loss.
Huang BQ et al.
Journal of Otology, 2015
Identification of a novel mutation in POU3F4 for prenatal diagnosis in a Chinese family with X-linked nonsyndromic hearing loss.
Li J et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao, 2010
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