RNASEH2A
|
0.700 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1.
|
25604658 |
2015 |
RNASEH2A
|
0.700 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
A practical approach to diagnosing adult onset leukodystrophies.
|
24357685 |
2014 |
RNASEH2A
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
Assessment of interferon-related biomarkers in Aicardi-Goutières syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, and ADAR: a case-control study.
|
24183309 |
2013 |
RNASEH2A
|
0.700 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Functional consequences of the RNase H2A subunit mutations that cause Aicardi-Goutieres syndrome.
|
21454563 |
2011 |
RNASEH2A
|
0.700 |
GeneticVariation
|
disease |
UNIPROT |
Expanding the phenotypic spectrum of lupus erythematosus in Aicardi-Goutières syndrome.
|
20131292 |
2010 |
RNASEH2A
|
0.700 |
GeneticVariation
|
disease |
UNIPROT |
Clinical and molecular phenotype of Aicardi-Goutieres syndrome.
|
17846997 |
2007 |
RNASEH2A
|
0.700 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutières syndrome and mimic congenital viral brain infection.
|
16845400 |
2006 |
RNASEH2A
|
0.700 |
GeneticVariation
|
disease |
UNIPROT |
Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutières syndrome and mimic congenital viral brain infection.
|
16845400 |
2006 |
RNASEH2A
|
0.700 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Genetic syndromes mimic congenital infections.
|
15870678 |
2005 |
RNASEH2A
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
|
|
|
RNASEH2A
|
0.700 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
|
|
|
RNASEH2A
|
0.700 |
Biomarker
|
disease |
CTD_human |
|
|
|