|
| Entrez Id: |
51168 |
| Gene Symbol: |
MYO15A |
MYO15A
|
0.100 |
CausalMutation
|
group |
CLINVAR |
Mutational Spectrum of MYO15A and the Molecular Mechanisms of DFNB3 Human Deafness.
|
27375115 |
2016 |
|
| Entrez Id: |
51168 |
| Gene Symbol: |
MYO15A |
MYO15A
|
0.100 |
GeneticVariation
|
group |
CLINVAR |
Mutational Spectrum of MYO15A and the Molecular Mechanisms of DFNB3 Human Deafness.
|
27375115 |
2016 |
|
| Entrez Id: |
51168 |
| Gene Symbol: |
MYO15A |
MYO15A
|
0.100 |
GeneticVariation
|
group |
CLINVAR |
Identification and Clinical Implications of Novel MYO15A Mutations in a Non-consanguineous Korean Family by Targeted Exome Sequencing.
|
26242193 |
2015 |
|
| Entrez Id: |
51168 |
| Gene Symbol: |
MYO15A |
MYO15A
|
0.100 |
CausalMutation
|
group |
CLINVAR |
Mutations in the MYO15A gene are a significant cause of nonsyndromic hearing loss: massively parallel DNA sequencing-based analysis.
|
25792667 |
2015 |
|
| Entrez Id: |
51168 |
| Gene Symbol: |
MYO15A |
MYO15A
|
0.100 |
CausalMutation
|
group |
CLINVAR |
Identification and Clinical Implications of Novel MYO15A Mutations in a Non-consanguineous Korean Family by Targeted Exome Sequencing.
|
26242193 |
2015 |
|
| Entrez Id: |
51168 |
| Gene Symbol: |
MYO15A |
MYO15A
|
0.100 |
GeneticVariation
|
group |
CLINVAR |
Mutations in the MYO15A gene are a significant cause of nonsyndromic hearing loss: massively parallel DNA sequencing-based analysis.
|
25792667 |
2015 |
|
| Entrez Id: |
51168 |
| Gene Symbol: |
MYO15A |
MYO15A
|
0.100 |
CausalMutation
|
group |
CLINVAR |
Forty-six genes causing nonsyndromic hearing impairment: which ones should be analyzed in DNA diagnostics?
|
18804553 |
2009 |
|
| Entrez Id: |
51168 |
| Gene Symbol: |
MYO15A |
MYO15A
|
0.100 |
GeneticVariation
|
group |
CLINVAR |
Forty-six genes causing nonsyndromic hearing impairment: which ones should be analyzed in DNA diagnostics?
|
18804553 |
2009 |
|
| Entrez Id: |
51168 |
| Gene Symbol: |
MYO15A |
MYO15A
|
0.100 |
GeneticVariation
|
group |
CLINVAR |
A gene for congenital, recessive deafness DFNB3 maps to the pericentromeric region of chromosome 17.
|
7704031 |
1995 |
|
| Entrez Id: |
51168 |
| Gene Symbol: |
MYO15A |
MYO15A
|
0.100 |
GeneticVariation
|
group |
CLINVAR |
Congenital non-syndromal autosomal recessive deafness in Bengkala, an isolated Balinese village.
|
7616538 |
1995 |
|
| Entrez Id: |
51168 |
| Gene Symbol: |
MYO15A |
MYO15A
|
0.100 |
CausalMutation
|
group |
CLINVAR |
A gene for congenital, recessive deafness DFNB3 maps to the pericentromeric region of chromosome 17.
|
7704031 |
1995 |
|
| Entrez Id: |
51168 |
| Gene Symbol: |
MYO15A |
MYO15A
|
0.100 |
CausalMutation
|
group |
CLINVAR |
Congenital non-syndromal autosomal recessive deafness in Bengkala, an isolated Balinese village.
|
7616538 |
1995 |