rs137853285
|
|
Hepatolenticular Degeneration
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
|
27854360 |
2017 |
rs137853285
|
|
Hepatolenticular Degeneration
|
T |
0.800 |
CausalMutation
|
CLINVAR |
Mutational analysis of ATP7B in Chinese Wilson disease patients.
|
27398169 |
2016 |
rs137853285
|
|
Hepatolenticular Degeneration
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Spectrum of mutations in the ATP binding domain of ATP7B gene of Wilson Disease in a regional Indian cohort.
|
25982861 |
2015 |
rs137853285
|
|
Hepatolenticular Degeneration
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Evidence for synergistic effects of PRNP and ATP7B mutations in severe neuropsychiatric deterioration.
|
24555712 |
2014 |
rs137853285
|
|
Hepatolenticular Degeneration
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Distinct phenotype of a Wilson disease mutation reveals a novel trafficking determinant in the copper transporter ATP7B.
|
24706876 |
2014 |
rs137853285
|
|
Hepatolenticular Degeneration
|
|
0.800 |
GeneticVariation
|
UNIPROT |
A new ATP7B gene mutation with severe condition in two unrelated Iranian families with Wilson disease.
|
23159873 |
2013 |
rs137853285
|
|
Hepatolenticular Degeneration
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Mutational analysis of ATP7B in north Chinese patients with Wilson disease.
|
23235335 |
2013 |
rs137853285
|
|
Hepatolenticular Degeneration
|
|
0.800 |
GeneticVariation
|
UNIPROT |
A genetic study of Wilson's disease in the United Kingdom.
|
23518715 |
2013 |
rs137853285
|
|
Hepatolenticular Degeneration
|
T |
0.800 |
CausalMutation
|
CLINVAR |
Mutation analysis of ATP7B gene in Turkish Wilson disease patients: identification of five novel mutations.
|
23333878 |
2013 |
rs137853285
|
|
Hepatolenticular Degeneration
|
T |
0.800 |
CausalMutation
|
CLINVAR |
Diverse functional properties of Wilson disease ATP7B variants.
|
22240481 |
2012 |
rs137853285
|
|
Hepatolenticular Degeneration
|
|
0.800 |
GeneticVariation
|
UNIPROT |
New novel mutation of the ATP7B gene in a family with Wilson disease.
|
22075048 |
2012 |
rs137853285
|
|
Hepatolenticular Degeneration
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Identification of a novel Wilson disease gene mutation frequent in Upper Austria: a genetic and clinical study.
|
22763723 |
2012 |
rs137853285
|
|
Hepatolenticular Degeneration
|
|
0.800 |
GeneticVariation
|
UNIPROT |
EFNS guidelines on diagnosis and treatment of primary dystonias.
|
20482602 |
2011 |
rs137853285
|
|
Hepatolenticular Degeneration
|
T |
0.800 |
CausalMutation
|
CLINVAR |
Hepatocyte GP73 expression in Wilson disease.
|
19596473 |
2009 |
rs137853285
|
|
Hepatolenticular Degeneration
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Diagnosis and treatment of Wilson disease: an update.
|
18506894 |
2008 |
rs137853285
|
|
Hepatolenticular Degeneration
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Twenty-four novel mutations in Wilson disease patients of predominantly Italian origin.
|
17949296 |
2007 |
rs137853285
|
|
Hepatolenticular Degeneration
|
T |
0.800 |
CausalMutation
|
CLINVAR |
Distinct Wilson's disease mutations in ATP7B are associated with enhanced binding to COMMD1 and reduced stability of ATP7B.
|
17919502 |
2007 |
rs137853285
|
|
Hepatolenticular Degeneration
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Distinct Wilson's disease mutations in ATP7B are associated with enhanced binding to COMMD1 and reduced stability of ATP7B.
|
17919502 |
2007 |
rs137853285
|
|
Hepatolenticular Degeneration
|
T |
0.800 |
CausalMutation
|
CLINVAR |
Late-onset Wilson's disease.
|
17433323 |
2007 |
rs137853285
|
|
Hepatolenticular Degeneration
|
T |
0.800 |
CausalMutation
|
CLINVAR |
Mutation analysis of the ATP7B gene and genotype/phenotype correlation in 227 patients with Wilson disease.
|
15967699 |
2006 |
rs137853285
|
|
Hepatolenticular Degeneration
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Mutation analysis of the ATP7B gene and genotype/phenotype correlation in 227 patients with Wilson disease.
|
15967699 |
2006 |
rs137853285
|
|
Hepatolenticular Degeneration
|
T |
0.800 |
CausalMutation
|
CLINVAR |
Molecular pathogenesis of Wilson disease: haplotype analysis, detection of prevalent mutations and genotype-phenotype correlation in Indian patients.
|
16133174 |
2005 |
rs137853285
|
|
Hepatolenticular Degeneration
|
T |
0.800 |
CausalMutation
|
CLINVAR |
Wilson's Disease.
|
16233999 |
2005 |
rs137853285
|
|
Hepatolenticular Degeneration
|
T |
0.800 |
CausalMutation
|
CLINVAR |
Defective cellular localization of mutant ATP7B in Wilson's disease patients and hepatoma cell lines.
|
12557139 |
2003 |
rs137853285
|
|
Hepatolenticular Degeneration
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Abnormal mRNA splicing resulting from consensus sequence splicing mutations of ATP7B.
|
12325021 |
2002 |