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A multimorphic mutation in IRF4 causes human autosomal dominant combined immunodeficiency

by Fornes, Oriol, Jia, Alicia, Kuehn, Hye Sun, Min, Qing, Pannicke, Ulrich, Schleussner, Nikolai, Thouenon, Romane, Yu, Zhijia, de Los Angeles Astbury, María, Biggs, Catherine M, Galicchio, Miguel, Garcia-Campos, Jorge Alberto, Gismondi, Silvina, Gonzalez Villarreal, Guadalupe, Hildebrand, Kyla J, Hönig, Manfred, Hou, Jia, Moshous, Despina, Pittaluga, Stefania, Qian, Xiaowen, Rozmus, Jacob, Schulz, Ansgar S, Staines-Boone, Aidé Tamara, Sun, Bijun, Sun, Jinqiao, Uwe, Schauer, Venegas-Montoya, Edna, Wang, Wenjie, Wang, Xiaochuan, Ying, Wenjing, Zhai, Xiaowen, Zhou, Qinhua, Akalin, Altuna, André, Isabelle, Barth, Thomas F E, Baumann, Bernd, Brüstle, Anne, Burgio, Gaetan, Bustamante, Jacinta C, Casanova, Jean-Laurent, Casarotto, Marco G, Cavazzana, Marina, Chentout, Loïc, Cockburn, Ian A, Costanza, Mariantonia, Cui, Chaoqun, Daumke, Oliver, Del Bel, Kate L, Eibel, Hermann, Feng, Xiaoqian, Franke, Vedran, Gebhardt, J Christof M, Götz, Andrea, Grunwald, Stephan, Hoareau, Bénédicte, Hughes, Timothy R, Jacobsen, Eva-Maria, Janz, Martin, Jolma, Arttu, Lagresle-Peyrou, Chantal, Lai, Nannan, Li, Yaxuan, Lin, Susan, Lu, Henry Y, Lugo-Reyes, Saul O, Meng, Xin, Möller, Peter, Moreno-Corona, Nidia, Niemela, Julie E, Novakovsky, Gherman, Perez-Caraballo, Jareb J, Picard, Capucine, Poggi, Lucie, Puig-Lombardi, Maria-Emilia, Randall, Katrina L, Reisser, Anja, Schmitt, Yohann, Seneviratne, Sandali, Sharma, Mehul, Stoddard, Jennifer, Sundararaj, Srinivasan, Sutton, Harry, Tran, Linh Q, Wang, Ying, Wasserman, Wyeth W, Wen, Zichao, Winkler, Wiebke, Xiong, Ermeng, Yang, Ally W H, Yu, Meiping, Zhang, Lumin, Zhang, Hai, Zhao, Qian, Zhen, Xin, Enders, Anselm, Kracker, Sven, Martinez-Barricarte, Ruben, Mathas, Stephan, Rosenzweig, Sergio D, Schwarz, Klaus
Published in Science immunology (20.01.2023)

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