Mutations in ADAR1 cause Aicardi-Goutières syndrome associated with a type I interferon signature.

Rice GI;Kasher PR;Forte GM;Mannion NM;Greenwood SM;Szynkiewicz M.;Dickerson JE;Bhaskar SS;Zampini M.;Briggs TA;Jenkinson EM;Bacino CA;Battini R.;Bertini E.;Brogan PA;Brueton LA;Carpanelli M.;De Laet C.;de Lonlay P.;Del Toro M.;Desguerre I.;FAZZI, Elisa Maria;Garcia Cazorla A.;Heiberg A.;Kawaguchi M.;Kumar R.;Lin JP;Lourenco CM;Male AM;Marques W. Jr;Mignot C.;Olivieri I.;Orcesi S.;Prabhakar P.;Rasmussen M.;Robinson RA;Rozenberg F.;Schmidt JL;Steindl K.;Tan TY;van der Merwe WG;Vanderver A.;Vassallo G.;Wakeling EL;Wassmer E.;Whittaker E.;Livingston JH;Lebon P.;Suzuki T.;McLaughlin PJ;Keegan LP;O'Connell MA;Lovell SC;Crow YJ

2012-01-01