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Assessment of interferon-related biomarkers in Aicardi-Goutières syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, and ADAR: a case-control study.

par Rice, Gillian I;Forte, Gabriella M A GM;Szynkiewicz, Marcin;Chase, Diana S;Aeby, Alec ;Abdel Hamid, Mohamed;Ackroyd, Sam;Allcock, Rebecca;Bailey, Kathryn M;Balottin, Umberto;Barnerias, Christine;Bernard, Genevieve;Bodemer, Christine;Botella, Maria P;Cereda, Cristina;Chandler, Kate K.E.;Dabydeen, Lyvia;Dale, Russell C;De Laet, Corinne ;De Goede, Christian G E L CG;Del Toro, Mireia;Effat, Laila;Enamorado, Noemi Nunez;Fazzi, Elisa;Gener, Blanca ;Haldre, Madli;Lin, Jean-Pierre S-M JP;Livingston, John JH;Lourenco, Charles Marques;Marques, Wilson;Oades, Patrick;Peterson, Pärt;Rasmussen, Magnhild;Roubertie, Agathe;Schmidt, Johanna Loewenstein;Shalev, Stavit A;Simon, Rogelio;Spiegel, Ronen;Swoboda, Kathryn KJ;Temtamy, Samia SA;Vassallo, Grace;Vilain, Catheline ;Vogt, Julie;Wermenbol, Vanessa ;Whitehouse, William WP;Soler, Doriette M;Olivieri, I.;Orcesi, Simona;Aglan, Mona MS;Zaki, Maha S;Abdel-Salam, Ghada M H;Vanderver, Adeline;Kisand, Kai;Rozenberg, Flore;Lebon, Pierre;Crow, Yanick J
Référence Lancet neurology, 12, 12, page (1159-1169)
Publication Publié, 2013-12

Article révisé par les pairs

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