Complete human CD1a deficiency on Langerhans cells due to a rare point mutation in the coding sequence

Por Cerny, Daniela, Thi Le, Duyen Huynh, The, Trung Dinh, Zuest, Roland, KG, Srinivasan, Velumani, Sumathy, Khor, Chiea Chuen, Mori, Lucia, Simmons, Cameron P., Poidinger, Michael, Zolezzi, Francesca, Ginhoux, Florent, Haniffa, Muzlifah, Wills, Bridget, Fink, Katja
Publicado no J Allergy Clin Immunol (2016)