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Elsevier, Clinical Immunology, (208), p. 108228, 2019

DOI: 10.1016/j.clim.2019.06.004

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Profound immunodeficiency with severe skin disease explained by concomitant novel CARMIL2 and PLEC1 loss-of-function mutations

Journal article published in 2019 by Maria E. Maccari, Carsten Speckmann, Maximilian Heeg, Antonia Reimer ORCID, Federica Casetti, Cristina Has, Stephan Ehl, Carla N. Castro
This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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