T-cell defects in patients with ARPC1B germline mutations account for combined immunodeficiency
- Resource Type
- Article
- Authors
- Brigida, Immacolata; Zoccolillo, Matteo; Cicalese, Maria Pia; Pfajfer, Laurène; Barzaghi, Federica; Scala, Serena; Oleaga-Quintas, Carmen; Álvarez-Álvarez, Jesus A.; Sereni, Lucia; Giannelli, Stefania; Sartirana, Claudia; Dionisio, Francesca; Pavesi, Luca; Benavides-Nieto, Marta; Basso-Ricci, Luca; Capasso, Paola; Mazzi, Benedetta; Rosain, Jeremie; Marcus, Nufar; Lee, Yu Nee; Somech, Raz; Degano, Massimo; Raiola, Giuseppe; Caorsi, Roberta; Picco, Paolo; Moncada Velez, Marcela; Khourieh, Joelle; Arias, Andrés Augusto; Bousfiha, Aziz; Issekutz, Thomas; Issekutz, Andrew; Boisson, Bertrand; Dobbs, Kerry; Villa, Anna; Lombardo, Angelo; Neven, Benedicte; Moshous, Despina; Casanova, Jean-Laurent; Franco, José Luis; Notarangelo, Luigi D.; Scielzo, Cristina; Volpi, Stefano; Dupré, Loïc; Bustamante, Jacinta; Gattorno, Marco ; Aiuti, Alessandro
- Source
- In Blood 29 November 2018 132(22):2362-2374
- Subject
- Language
- ISSN
- 0006-4971