Generation of three iPSC lines from fibroblasts of a patient with Aicardi Goutières Syndrome mutated in TREX1
Rosalba Monica Ferraro(Azienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia), Silvia Giliani(Azienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia), Jessica Galli(Azienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia), Gaetana Lanzi(Azienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia), Stefania Masneri(University of Brescia), Chiara Barisani(University of Brescia), Giovanna Piovani(University of Brescia), Elisa Fazzi(Centro Studi GISED), Marco Cattalini(University of Brescia), Marco Muzi-Falconi(University of Milan), Simona Orcesi(Fondazione Istituto Neurologico Nazionale Casimiro Mondino), Giulia Savio(University of Brescia), Cristina Cereda(University of Milan)
Cited by 12
Related Papers
Characterization of human disease phenotypes associated with mutations in <i>TREX1</i>, <i>RNASEH2A</i>, <i>RNASEH2B</i>, <i>RNASEH2C</i>, <i>SAMHD1</i>, <i>ADAR</i>, and <i>IFIH1</i>
|American Journal of Medical Genetics Part A|2015|617
Drug Retention Rate and Predictive Factors of Drug Survival for Interleukin-1 Inhibitors in Systemic Juvenile Idiopathic Arthritis
|Frontiers in Pharmacology|2019|616
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
|Nature Genetics|2021|567