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Journal Journal of Allergy and Clinical Immunology
Geelen, J, Pfundt, R, Meijer, J, Verheijen, F.W, & van Kuilenburg, A.B.P. (2013). Severe phenotype of severe combined immunodeficiency caused by adenosine deaminase deficiency in a patient with a homozygous mutation due to uniparental disomy. Journal of Allergy and Clinical Immunology, 132(1), 222–223. doi:10.1016/j.jaci.2012.11.006