Deafness, Autosomal Dominant 10
|
0.730 |
GeneticVariation
|
disease |
CLINVAR |
Exome sequencing reveals novel variants and unique allelic spectrum for hearing impairment in Filipino cochlear implantees.
|
30828794 |
2019 |
Deafness, Autosomal Dominant 10
|
0.730 |
Biomarker
|
disease |
BEFREE |
Only four genetic midfrequency deafness genes, namely, DFNA10 (EYA4), DFNA8/12 (TECTA), DFNA13 (COL11A2), DFNA44 (CCDC50), have been reported to date.
|
27142990 |
2016 |
Deafness, Autosomal Dominant 10
|
0.730 |
GeneticVariation
|
disease |
BEFREE |
A mutation in EYA4 was found in a Dutch family, causing DFNA10.
|
26331839 |
2016 |
Deafness, Autosomal Dominant 10
|
0.730 |
GeneticVariation
|
disease |
CLINVAR |
Evaluation of the contribution of the EYA4 and GRHL2 genes in Korean patients with autosomal dominant non-syndromic hearing loss.
|
25781927 |
2015 |
Deafness, Autosomal Dominant 10
|
0.730 |
GeneticVariation
|
disease |
UNIPROT |
Exome Sequencing Identifies a Mutation in EYA4 as a Novel Cause of Autosomal Dominant Non-Syndromic Hearing Loss.
|
25961296 |
2015 |
Deafness, Autosomal Dominant 10
|
0.730 |
GeneticVariation
|
disease |
UNIPROT |
A novel mutation of EYA4 in a large Chinese family with autosomal dominant middle-frequency sensorineural hearing loss by targeted exome sequencing.
|
25809937 |
2015 |
Deafness, Autosomal Dominant 10
|
0.730 |
GeneticVariation
|
disease |
UNIPROT |
Targeted massive parallel sequencing: the effective detection of novel causative mutations associated with hearing loss in small families.
|
22938506 |
2012 |
Deafness, Autosomal Dominant 10
|
0.730 |
GeneticVariation
|
disease |
CLINVAR |
Nonsyndromic hearing loss DFNA10 and a novel mutation of EYA4: evidence for correlation of normal cardiac phenotype with truncating mutations of the Eya domain.
|
17567890 |
2007 |
Deafness, Autosomal Dominant 10
|
0.730 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Mutation in the transcriptional coactivator EYA4 causes dilated cardiomyopathy and sensorineural hearing loss.
|
15735644 |
2005 |
Deafness, Autosomal Dominant 10
|
0.730 |
GeneticVariation
|
disease |
CLINVAR |
Mutation in the transcriptional coactivator EYA4 causes dilated cardiomyopathy and sensorineural hearing loss.
|
15735644 |
2005 |
Deafness, Autosomal Dominant 10
|
0.730 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Mutation in the transcriptional coactivator EYA4 causes dilated cardiomyopathy and sensorineural hearing loss.
|
15735644 |
2005 |
Deafness, Autosomal Dominant 10
|
0.730 |
GeneticVariation
|
disease |
CLINVAR |
Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locus.
|
11159937 |
2001 |
Deafness, Autosomal Dominant 10
|
0.730 |
GeneticVariation
|
disease |
BEFREE |
We present a detailed analysis of the DFNA10 phenotype based on data from 25 hearing-impaired persons coming from a large American pedigree segregating for deafness at the DFNA10 locus (chromosome 6q22.3-23.2).
|
11558763 |
2001 |
Deafness, Autosomal Dominant 10
|
0.730 |
GeneticVariation
|
disease |
UNIPROT |
Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locus.
|
11159937 |
2001 |
Deafness, Autosomal Dominant 10
|
0.730 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
EYA4, a novel vertebrate gene related to Drosophila eyes absent.
|
9887327 |
1999 |
Deafness, Autosomal Dominant 10
|
0.730 |
CausalMutation
|
disease |
CLINVAR |
|
|
|
Deafness, Autosomal Dominant 10
|
0.730 |
Biomarker
|
disease |
CTD_human |
|
|
|