Associated Papers
Genetic analysis of patients with low-frequency non-syndromic hearing loss.
Yu S et al.
Molecular Genetics and Genomics : Mgg, 2024
Global Distribution of Founder Variants Associated with Non-Syndromic Hearing Impairment.
Aboagye ET et al.
Genes, 2023
Identification of a novel CNV at the EYA4 gene in a Chinese family with autosomal dominant nonsyndromic hearing loss.
Zhang W et al.
Bmc Medical Genomics, 2022
The genetic etiology of hearing loss in Japan revealed by the social health insurance-based genetic testing of 10K patients.
Usami SI et al.
Human Genetics, 2022
34599366 (PubMed )
Supplement: 439_2021_2371_MOESM2_ESM.xlsx › SuppleTable2_20210811_final
Identification of a Novel Copy Number Variation of EYA4 Causing Autosomal Dominant Non-syndromic Hearing Loss.
Ishino T et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology, 2021
Early truncation of the N-terminal variable region of EYA4 gene causes dominant hearing loss without cardiac phenotype.
Mi Y et al.
Molecular Genetics & Genomic Medicine, 2021
Insights into the pathophysiology of DFNA10 hearing loss associated with novel EYA4 variants.
Morín M et al.
Scientific Reports, 2020
Prevalence and clinical features of hearing loss caused by EYA4 variants.
Shinagawa J et al.
Scientific Reports, 2020
Novel EYA4 variant in Slovak family with late onset autosomal dominant hearing loss: a case report.
Varga L et al.
Bmc Medical Genetics, 2019
Identification of a novel missense eya4 mutation causing autosomal dominant non‑syndromic hearing loss in a chinese family.
Xiao SY et al.
Cellular and Molecular Biology (noisy-le-grand, France), 2019
Sensorineural hearing loss and mild cardiac phenotype caused by an EYA4 mutation.
Abe S et al.
Human Genome Variation, 2018
Evaluation of the contribution of the EYA4 and GRHL2 genes in Korean patients with autosomal dominant non-syndromic hearing loss.
Kim YR et al.
Plos One, 2015
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