Additional Metadata
Persistent URL dx.doi.org/10.1016/j.jaci.2012.11.006, hdl.handle.net/1765/52759
Journal Journal of Allergy and Clinical Immunology
Citation
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