rs111033233
×
Entrez Id:
4647
Gene Symbol:
MYO7A
MYO7A
Usher Syndrome, Type I
0.700
GeneticVariation
UNIPROT
Whole exome sequencing identifies mutations in Usher syndrome genes in profoundly deaf Tunisian patients.
25798947
2015
rs111033233
×
Entrez Id:
4647
Gene Symbol:
MYO7A
MYO7A
Usher Syndrome, Type I
0.700
GeneticVariation
UNIPROT
Novel and recurrent MYO7A mutations in Usher syndrome type 1 and type 2.
24831256
2014
rs111033233
×
Entrez Id:
4647
Gene Symbol:
MYO7A
MYO7A
Usher Syndrome, Type I
0.700
GeneticVariation
UNIPROT
Novel compound heterozygous mutations in MYO7A in a Chinese family with Usher syndrome type 1.
23559863
2013
rs111033233
×
Entrez Id:
4647
Gene Symbol:
MYO7A
MYO7A
Usher Syndrome, Type I
0.700
GeneticVariation
UNIPROT
Survey of the frequency of USH1 gene mutations in a cohort of Usher patients shows the importance of cadherin 23 and protocadherin 15 genes and establishes a detection rate of above 90%.
16679490
2006
rs111033233
×
Entrez Id:
4647
Gene Symbol:
MYO7A
MYO7A
Usher Syndrome, Type I
0.700
GeneticVariation
UNIPROT
Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient population.
15660226
2005
rs111033233
×
Entrez Id:
4647
Gene Symbol:
MYO7A
MYO7A
Usher Syndrome, Type I
0.700
GeneticVariation
UNIPROT
Mutations in myosin VIIA (MYO7A) and usherin (USH2A) in Spanish patients with Usher syndrome types I and II, respectively.
12112664
2002
rs111033233
×
Entrez Id:
4647
Gene Symbol:
MYO7A
MYO7A
Usher Syndrome, Type I
0.700
GeneticVariation
UNIPROT
Evaluation of the myosin VIIA gene and visual function in patients with Usher syndrome type I.
10930322
2000
rs111033233
×
Entrez Id:
4647
Gene Symbol:
MYO7A
MYO7A
Usher Syndrome, Type I
0.700
GeneticVariation
UNIPROT
Twelve novel myosin VIIA mutations in 34 patients with Usher syndrome type I: confirmation of genetic heterogeneity.
10094549
1999
rs111033233
×
Entrez Id:
4647
Gene Symbol:
MYO7A
MYO7A
Usher Syndrome, Type I
0.700
GeneticVariation
UNIPROT
Possible interaction between USH1B and USH3 gene products as implied by apparent digenic deafness inheritance.
10364543
1999
rs111033233
×
Entrez Id:
4647
Gene Symbol:
MYO7A
MYO7A
Usher Syndrome, Type I
0.700
GeneticVariation
UNIPROT
Identification of three novel mutations in the MYO7A gene.
10447383
1999
rs111033233
×
Entrez Id:
4647
Gene Symbol:
MYO7A
MYO7A
Usher Syndrome, Type I
0.700
GeneticVariation
UNIPROT
Mutations in the myosin VIIA gene cause a wide phenotypic spectrum, including atypical Usher syndrome.
9718356
1998
rs111033233
×
Entrez Id:
4647
Gene Symbol:
MYO7A
MYO7A
Usher Syndrome, Type I
0.700
GeneticVariation
UNIPROT
Myosin VIIA gene: heterogeneity of the mutations responsible for Usher syndrome type IB.
9002678
1997
rs111033233
×
Entrez Id:
4647
Gene Symbol:
MYO7A
MYO7A
Usher Syndrome, Type I
0.700
GeneticVariation
UNIPROT
Mutation profile of all 49 exons of the human myosin VIIA gene, and haplotype analysis, in Usher 1B families from diverse origins.
9382091
1997
rs111033233
×
Entrez Id:
4647
Gene Symbol:
MYO7A
MYO7A
Usher Syndrome, Type I
0.700
GeneticVariation
UNIPROT
Myosin VIIA mutation screening in 189 Usher syndrome type 1 patients.
8900236
1996
rs111033233
×
Entrez Id:
4647
Gene Symbol:
MYO7A
MYO7A
Usher Syndrome, Type I
0.700
GeneticVariation
UNIPROT
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
7870171
1995