Condition: Deafness, Autosomal Dominant 10


rs143936434 in EYA4 gene and Deafness, Autosomal Dominant 10 PMID 30828794 2019 Exome sequencing reveals novel variants and unique allelic spectrum for hearing impairment in Filipino cochlear implantees.

rs1562505728 in EYA4;TARID gene and Deafness, Autosomal Dominant 10 PMID 15735644 2005 Mutation in the transcriptional coactivator EYA4 causes dilated cardiomyopathy and sensorineural hearing loss.

PMID 11159937 2001 Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locus.

PMID 17567890 2007 Nonsyndromic hearing loss DFNA10 and a novel mutation of EYA4: evidence for correlation of normal cardiac phenotype with truncating mutations of the Eya domain.

PMID 25781927 2015 Evaluation of the contribution of the EYA4 and GRHL2 genes in Korean patients with autosomal dominant non-syndromic hearing loss.

rs797045088 in TARID;EYA4 gene and Deafness, Autosomal Dominant 10 PMID 11159937 2001 Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locus.