Complete human CD1a deficiency on Langerhans cells due to a rare point mutation in the coding sequence.
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.
Cerny D, et al. Among authors: velumani s.
J Allergy Clin Immunol. 2016 Dec;138(6):1709-1712.e11. doi: 10.1016/j.jaci.2016.05.028. Epub 2016 Jun 29.
J Allergy Clin Immunol. 2016.
PMID: 27484031
Free PMC article.
No abstract available.