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RNASEH2B gene

Known as: RNASEH2B, FLJ11712, RIBONUCLEASE H2, SUBUNIT B 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
SIGNIFICANCE OF TARGETED EXOME SEQUENCING AND METHODS OF DATA ANALYSIS IN THE DIAGNOSIS OF GENETIC DISORDERS LEADING TO THE DEVELOPMENT OF EPILEPTIC ENCEPHALOPATHY
Epilepsy is the most common serious neurological disorder, and there is a genetic basis in almost 50% of people with epilepsy… 
2014
2014
Autosomal dominant IFIH1 gain‐of‐function mutations cause Aicardi–Goutières syndrome
Aicardi–Goutières Syndrome is caused by IFIH1 mutations 
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