Severe phenotype of severe combined immunodeficiency caused by adenosine deaminase deficiency in a patient with a homozygous mutation due to uniparental disomy

2013-07-01

Additional Metadata
Persistent URL	doi.org/10.1016/j.jaci.2012.11.006, hdl.handle.net/1765/52759
Journal	Journal of Allergy and Clinical Immunology
Organisation	Department of Clinical Genetics
Citation APA Style AAA Style APA Style Cell Style Chicago Style Harvard Style IEEE Style MLA Style Nature Style Vancouver Style American-Institute-of-Physics Style Council-of-Science-Editors Style BibTex Format Endnote Format RIS Format CSL Format DOIs only Format	Geelen, J., Pfundt, R., Meijer, J., Verheijen, F., & van Kuilenburg, A. (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

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