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

Daniela Cerny; Duyen Huynh Thi Le; Trung Dinh The; Roland Zuest; Srinivasan KG; Sumathy Velumani; Chiea Chuen Khor; Lucia Mori; Cameron P. Simmons; Michael Poidinger; Francesca Zolezzi; Florent Ginhoux; Muzlifah Haniffa; Bridget Wills; Katja Fink

doi:10.1016/j.jaci.2016.05.028

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

Daniela Cerny, Duyen Huynh Thi Le, Trung Dinh The, Roland Zuest, Srinivasan KG, Sumathy Velumani, Chiea Chuen Khor, Lucia Mori, Cameron P. Simmons, Michael Poidinger, Francesca Zolezzi, Florent Ginhoux, Muzlifah Haniffa, Bridget Wills, Katja Fink

Research output: Contribution to journal › Article › peer-review

3 Citations (Scopus)

Original language	English
Pages (from-to)	1709-1712.e11
Journal	Journal of Allergy and Clinical Immunology
Volume	138
Issue number	6
DOIs	https://doi.org/10.1016/j.jaci.2016.05.028
Publication status	Published - 1 Dec 2016
Externally published	Yes

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10.1016/j.jaci.2016.05.028

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Cerny, D., Thi Le, D. H., The, T. D., Zuest, R., KG, S., Velumani, S., Khor, C. C., Mori, L., Simmons, C. P., Poidinger, M., Zolezzi, F., Ginhoux, F., Haniffa, M., Wills, B., & Fink, K. (2016). Complete human CD1a deficiency on Langerhans cells due to a rare point mutation in the coding sequence. Journal of Allergy and Clinical Immunology, 138(6), 1709-1712.e11. https://doi.org/10.1016/j.jaci.2016.05.028

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

author = "Daniela Cerny and {Thi Le}, {Duyen Huynh} and The, {Trung Dinh} and Roland Zuest and Srinivasan KG and Sumathy Velumani and Khor, {Chiea Chuen} and Lucia Mori and Simmons, {Cameron P.} and Michael Poidinger and Francesca Zolezzi and Florent Ginhoux and Muzlifah Haniffa and Bridget Wills and Katja Fink",

note = "Funding Information: This work was funded by the Agency for Science, Technology and Research A*STAR and by the Wellcome Trust. ",

year = "2016",

month = dec,

day = "1",

doi = "10.1016/j.jaci.2016.05.028",

language = "English",

volume = "138",

pages = "1709--1712.e11",

journal = "Journal of Allergy and Clinical Immunology",

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Cerny, D, Thi Le, DH, The, TD, Zuest, R, KG, S, Velumani, S, Khor, CC, Mori, L, Simmons, CP, Poidinger, M, Zolezzi, F, Ginhoux, F, Haniffa, M, Wills, B & Fink, K 2016, 'Complete human CD1a deficiency on Langerhans cells due to a rare point mutation in the coding sequence', Journal of Allergy and Clinical Immunology, vol. 138, no. 6, pp. 1709-1712.e11. https://doi.org/10.1016/j.jaci.2016.05.028

TY - JOUR

T1 - Complete human CD1a deficiency on Langerhans cells due to a rare point mutation in the coding sequence

AU - Cerny, Daniela

AU - Thi Le, Duyen Huynh

AU - The, Trung Dinh

AU - Zuest, Roland

AU - KG, Srinivasan

AU - Velumani, Sumathy

AU - Khor, Chiea Chuen

AU - Mori, Lucia

AU - Simmons, Cameron P.

AU - Poidinger, Michael

AU - Zolezzi, Francesca

AU - Ginhoux, Florent

AU - Haniffa, Muzlifah

AU - Wills, Bridget

AU - Fink, Katja

N1 - Funding Information: This work was funded by the Agency for Science, Technology and Research A*STAR and by the Wellcome Trust.

PY - 2016/12/1

Y1 - 2016/12/1

UR - http://www.scopus.com/inward/record.url?scp=84997764950&partnerID=8YFLogxK

U2 - 10.1016/j.jaci.2016.05.028

DO - 10.1016/j.jaci.2016.05.028

M3 - Article

C2 - 27484031

AN - SCOPUS:84997764950

SN - 0091-6749

VL - 138

SP - 1709-1712.e11

JO - Journal of Allergy and Clinical Immunology

JF - Journal of Allergy and Clinical Immunology

IS - 6

ER -

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

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