Subject
Neurology (clinical),Neurology,General Medicine
Reference43 articles.
1. A progressive familial encephalopathy in infancy with calcifications of the basal ganglia and chronic cerebrospinal fluid lymphocytosis;Aicardi;Ann Neurol,1984
2. Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1;Crow;Am J Med Genet A,2015
3. Aicardi-Goutières syndrome and the type I interferonopathies;Crow;Nat Rev Immunol,2015
4. Aicardi-Goutières syndrome;Orcesi;Br Med Bull,2009
5. Neurologic phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR1, and IFIH1: aicardi-goutières syndrome and beyond;Livingston;Neuropediatrics,2016
Cited by
2 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