Author:
Bamborschke Daniel,Kreutzer Mona,Koy Anne,Koerber Friederike,Lucas Nadja,Huenseler Christoph,Herkenrath Peter,Lee-Kirsch Min Ae,Cirak Sebahattin
Subject
Clinical Neurology,Developmental Neuroscience,General Medicine,Pediatrics, Perinatology, and Child Health
Reference20 articles.
1. The Type I Interferonopathies;Lee-Kirsch;Annu Rev Med,2017
2. Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1;Crow;Am J Med Genetics Part A,2015
3. Clinical spectrum and functional consequences associated with bi-allelic pathogenic PNPT1 variants;Rius;J Clin Med,2019
4. Mutation in PNPT1, which encodes a polyribonucleotide nucleotidyltransferase, impairs RNA import into mitochondria and causes respiratory-chain deficiency;Vedrenne;Am J Hum Genet,2012
5. Mitochondrial double-stranded RNA triggers antiviral signalling in humans;Dhir;Nature,2018
Cited by
22 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