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Elsevier, Journal of Allergy and Clinical Immunology, 6(138), p. 1709-1712.e11, 2016

DOI: 10.1016/j.jaci.2016.05.028

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

This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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