Associated Papers
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
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
Research progress in pathogenic genes of hereditary non-syndromic mid-frequency deafness.
Xia W et al.
Frontiers of Medicine, 2016
Identification of a novel truncation mutation of EYA4 in moderate degree hearing loss by targeted exome sequencing.
Choi HS et al.
European Archives of Oto-rhino-laryngology : Official Journal of the European Federation of Oto-rhino-laryngological Societies (eufos) : Affiliated With the German Society for Oto-rhino-laryngology - Head and Neck Surgery, 2016
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
Exome Sequencing Identifies a Mutation in EYA4 as a Novel Cause of Autosomal Dominant Non-Syndromic Hearing Loss.
Liu F et al.
Plos One, 2015
Nonsyndromic hearing loss DFNA10 and a novel mutation of EYA4: evidence for correlation of normal cardiac phenotype with truncating mutations of the Eya domain.
Makishima T et al.
American Journal of Medical Genetics. Part A, 2007
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