Complete human CD1a deficiency on Langerhans cells due to a rare point mutation in the coding sequence - 18/04/17

Doi : 10.1016/j.jaci.2016.05.028

Daniela Cerny, PhD ^a,^b, Duyen Huynh Thi Le, MSc ^c, Trung Dinh The, MD, PhD ^c, Roland Zuest, PhD ^a, Srinivasan KG, PhD ^a, Sumathy Velumani, MSc ^a, Chiea Chuen Khor, MD, PhD ^d, Lucia Mori, PhD ^a,^e, Cameron P. Simmons, PhD ^c,^f,^g, Michael Poidinger, PhD ^a, Francesca Zolezzi, PhD ^a, Florent Ginhoux, PhD ^a, Muzlifah Haniffa, MD, PhD ^h, Bridget Wills, MD, DM ^c,^f , Katja Fink, PhD ^a,^b
^a Singapore Immunology Network, A*STAR, Singapore
^b School of Biological Sciences, Nanyang Technological University, Singapore
^c Oxford University Clinical Research Unit, Hospital for Tropical Diseases, Ho Chi Minh City, Vietnam
^d Genome Institute of Singapore, A*STAR, Singapore
^e Experimental Immunology, Department of Biomedicine, University Hospital Basel, University of Basel, Basel, Switzerland
^f Nuffield Department of Clinical Medicine, Oxford University, Oxford, United Kingdom
^g Department of Microbiology and Immunology, University of Melbourne, the Peter Doherty Institute of Infection and Immunity, Carlton, Victoria, Australia
^h Institute of Cellular Medicine, Newcastle University, Newcastle, United Kingdom

	This work was funded by the Agency for Science, Technology and Research A*STAR and by the Wellcome Trust.
	Disclosure of potential conflict of interest: The authors declare that they have no relevant conflicts of interest.

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Vol 138 - N° 6

P. 1709 - décembre 2016 Retour au numéro

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Complete human CD1a deficiency on Langerhans cells due to a rare point mutation in the coding sequence - 18/04/17

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