Author:
Bartsch Kareen,Knittler Katharina,Borowski Christopher,Rudnik Sönke,Damme Markus,Aden Konrad,Spehlmann Martina E.,Frey Norbert,Saftig Paul,Chalaris Athena,Rabe Björn
Funder
Deutsche Forschungsgemeinschaft
Publisher
Oxford University Press (OUP)
Subject
Genetics(clinical),Genetics,Molecular Biology,General Medicine
Reference52 articles.
1. Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1;Am. J. Med. Genet. A,2015
2. Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutieres syndrome and mimic congenital viral brain infection;Nat. Genet,2006
3. Aicardi-Goutieres syndrome and the type I interferonopathies;Nat. Rev. Immunol,2015
4. Trex1 prevents cell-intrinsic initiation of autoimmunity;Cell,2008
5. Modulation of LINE-1 and Alu/SVA retrotransposition by Aicardi-Goutieres syndrome-related SAMHD1;Cell Rep,2013
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