Defective glycosylation and multisystem abnormalities characterize the primary immunodeficiency XMEN disease
Ravell, Juan C, Matsuda-Lennikov, Mami, Chauvin, Samuel D, Zou, Juan, Biancalana, Matthew, Deeb, Sally J, Price, Susan, Su, Helen C, Notarangelo, Giulia, Jiang, Ping, Morawski, Aaron, Kanellopoulou, Chrysi, Binder, Kyle, Mukherjee, Ratnadeep, Anibal, James T, Sellers, Brian, Zheng, Lixin, He, Tingyan, George, Alex B, Pittaluga, Stefania, Powers, Astin, Kleiner, David E, Kapuria, Devika, Ghany, Marc, Hunsberger, Sally, Cohen, Jeffrey I, Uzel, Gulbu, Bergerson, Jenna, Wolfe, Lynne, Toro, Camilo, Gahl, William, Folio, Les R, Matthews, Helen, Angelus, Pam, Chinn, Ivan K, Orange, Jordan S, Trujillo-Vargas, Claudia M, Franco, Jose Luis, Orrego-Arango, Julio, Gutiérrez-Hincapié, Sebastian, Patel, Niraj Chandrakant, Raymond, Kimiyo, Patiroglu, Turkan, Unal, Ekrem, Karakukcu, Musa, Day, Alexandre Gr, Mehta, Pankaj, Masutani, Evan, De Ravin, Suk S, Malech, Harry L, Altan-Bonnet, Grégoire, Rao, V Koneti, Mann, Matthias, Lenardo, Michael J
Published in The Journal of clinical investigation (01.01.2020)
Published in The Journal of clinical investigation (01.01.2020)
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