Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1

Crow, Yj;Chase, Ds;Lowenstein Schmidt, J;Szynkiewicz, M;Forte, Gm;Gornall, Hl;Oojageer, A;Anderson, B;Pizzino, A;Helman, G;Abdel Hamid, Ms;Abdel Salam, Gm;Ackroyd, S;Aeby, A;Agosta, G;Albin, C;Allon Shalev, S;Arellano, M;Ariaudo, G;Aswani, V;Babul Hirji, R;Baildam, Em;Bahi Buisson, N;Bailey, Km;Barnerias, C;Barth, M;Battini, R;Beresford, Mw;Bernard, G;Bianchi, M;Billette de Villemeur, T;Blair, Em;Bloom, M;Burlina, Ab;Carpanelli, Ml;Carvalho, Dr;Castro Gago, M;Cavallini, A;Cereda, C;Chandler, Ke;Chitayat, Da;Collins, Ae;Sierra Corcoles, C;Cordeiro, Nj;Crichiutti, G;Dabydeen, L;Dale, Rc;D'Arrigo, S;De Goede, Cg;De Laet, C;De Waele, Lm;Denzler, I;Desguerre, I;Devriendt, K;Di Rocco, M;Fahey, Mc;FAZZI, Elisa Maria;Ferrie, Cd;Figueiredo, A;Gener, B;Goizet, C;Gowrinathan, Nr;Gowrishankar, K;Hanrahan, D;Isidor, B;Kara, B;Khan, N;King, Md;Kirk, Ep;Kumar, R;Lagae, L;Landrieu, P;Lauffer, H;Laugel, V;La Piana, R;Lim, Mj;Lin, Jp;Linnankivi, T;Mackay, Mt;Marom, Dr;Marques Lourenço, C;Mckee, Sa;Moroni, I;Morton, Je;Moutard, Ml;Murray, K;Nabbout, R;Nampoothiri, S;Nunez Enamorado, N;Oades, Pj;Olivieri, I;Ostergaard, Jr;Pérez Dueñas, B;Prendiville, Js;Ramesh, V;Rasmussen, M;Régal, L;Ricci, F;Rio, M;Rodriguez, D;Roubertie, A;Salvatici, E;Segers, Ka;Sinha, Gp;Soler, D;Spiegel, R;Stödberg, Ti;Straussberg, R;Swoboda, Kj;Suri, M;Tacke, U;Tan, Ty;te Water Naude, J;Wee Teik, K;Thomas, Mm;Till, M;Tonduti, D;Valente, Em;Van Coster, Rn;van der Knaap, Ms;Vassallo, G;Vijzelaar, R;Vogt, J;Wallace, Gb;Wassmer, E;Webb, Hj;Whitehouse, Wp;Whitney, Rn;Zaki, Ms;Zuberi, Sm;Livingston, Jh;Rozenberg, F;Lebon, P;Vanderver, A;Orcesi, S;Rice, G.i.

2015-01-01