Characterization of Human Disease Phenotypes Associated with Mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1

Y.J. Crow, D.S. Chase, J.L. Schmidt, M. Szynkiewicz, G.M.A. Forte, H.L. Gornall, A. Oojageer, B. Anderson, A. Pizzino, G. Helman, M.S. Abdel-Hamid, G.M. Abdel-Salam, S. Ackroyd, A. Aeby, G. Agosta, C. Albin, S. Allon-Shalev, M. Arellano, G. Ariaudo, V. AswaniR. Babul-Hirji, E.M. Baildam, N. Bahi-Buisson, K.M. Bailey, C. Barnerias, M. Barth, R. Battini, M.W. Beresford, G. Bernard, M. Bianchi, T.B. de Villemeur, E.M. Blair, M. Bloom, A.B. Burlina, M.L. Carpanelli, D.R. Carvalho, M. Castro-Gago, A. Cavallini, C. Cereda, K.E. Chandler, D.A. Chitayat, A.E. Collins, C.S. Corcoles, N.J.V. Cordeiro, G. Crichiutti, L. Dabydeen, R.C. Dale, S. D'Arrigo, C.G.E.L. De Goede, C. de Laet, L.M.H. De Waele, I. Denzler, I. Desguerre, K. Devriendt, M. Di Rocco, M.C. Fahey, E. Fazzi, C.D. Ferrie, A. Figueiredo, B. Gener, C. Goizet, N.R. Gowrinathan, K. Gowrishankar, D. Hanrahan, B. Isidor, L. Kara, N. Khan, M.D. King, E.P. Kirk, R. Kumar, L. Lagae, P. Landrieu, H. Lauffer, V. Laugel, R. La Piana, M.J. Lim, J.P.S.M. Lin, T. Linnankivi, M.T. Mackay, D.R. Marom, C.M. Lourenco, S.A. McKee, I. Moroni, J.E.V. Morton, M.L. Moutard, K. Murray, R. Nabbout, S. Nampoothiri, N. Nunez-Enamorado, P.J. Oades, I. Olivieri, J.R. Ostergaard, B. Perez-Duenas, J.S. Prendiville, V. Ramesh, M. Rasmussen, L. Regal, F. Ricci, M. Rio, M. Knaap, S. Orcesi, G.I. Rice

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