Associated Papers
Clinical and Molecular Aspects Associated with Defects in the Transcription Factor POU3F4: A Review.
Bernardinelli E et al.
Biomedicines, 2023
Study of complex structural variations of X-linked deafness-2 based on single-molecule sequencing.
Jiang Y et al.
Bioscience Reports, 2021
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
Cochlear Implantation in a Patient with a Novel POU3F4 Mutation and Incomplete Partition Type-III Malformation.
Chao X et al.
Neural Plasticity, 2020
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