Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1.
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author: Yanick J. Crow, Diana Chase, Ghada M Abdel-Salam, Cristina Cereda, Michael Fahey, Elisa Fazzi, Jean-Pierre Lin, Davide Tonduti, Enza Maria Valente, William P Whitehouse, Maha Zaki, Adeline Vanderver, Gillian I. Rice, Guy Helman, Roberta Battini, Geneviève Bernard, Christian G E L de Goede, BELEN PEREZ DUEÑAS, Marlene Rio, Tiong Y Tan, Simona Orcesi, Kathryn J Swoboda, Ronen Spiegel, Manuel Castro-Gago, Roberta La Piana, Alec Aeby, Kate E Chandler, Corinne De Laet, Blanca Gener, Cyril Goizet, Marjo van der Knaap, Lieven Lagae, Daphna R Marom, Marie-Laure Moutard, Julie S Prendiville, Magnhild Rasmussen, Agathe Roubertie, Doriette M Soler, Uta Tacke, Evangeline Wassmer, Isabelle Desguerre, Hannah L Gornall, Pierre G Landrieu, Koenraad Devriendt, Gabriella M A Forte, Marcin Szynkiewicz, Ivana Olivieri, Flore Rozenberg, Grace Vassallo, David Chitayat, Riyana Babul-Hirji
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