Associated Papers
Genomic and phenotypic landscapes of X-linked hereditary hearing loss in the Chinese population.
Feng H et al.
Orphanet Journal of Rare Diseases, 2024
Clinical and Molecular Aspects Associated with Defects in the Transcription Factor POU3F4: A Review.
Bernardinelli E et al.
Biomedicines, 2023
Medical genetics and genomic medicine in Nigeria.
Adeyemo AA et al.
Molecular Genetics & Genomic Medicine, 2018
Novel domain-specific POU3F4 mutations are associated with X-linked deafness: examples from different populations.
Bademci G et al.
Bmc Medical Genetics, 2015
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