Author:
Schmelzer Lisa,Smitka Martin,Wolf Christine,Lucas Nadja,Tüngler Victoria,Hahn Gabriele,Tzschach Andreas,Di Donato Nataliya,Lee-Kirsch Min Ae,von der Hagen Maja
Funder
Deutsche Forschungsgemeinschaft
Subject
Neurology (clinical),General Medicine,Pediatrics, Perinatology and Child Health
Reference7 articles.
1. Aicardi-Goutieres syndrome and the type I interferonopathies;Crow;Nat Rev Immunol,2015
2. The type I interferonopathies;Lee-Kirsch;Annu Rev Med,2017
3. Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1;Crow;Am J Med Genet A,2015
4. Mutations in ADAR1 cause Aicardi-Goutieres syndrome associated with a type I interferon signature;Rice;Nat Genet,2012
5. Striking intrafamilial phenotypic variability in Aicardi-Goutieres syndrome associated with the recurrent Asian founder mutation in RNASEH2C;Vogt;Am J Med Genet A,2013
Cited by
18 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献