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

Joyce Geelen; Rolph Pfundt; Judith Meijer; Frans W Verheijen; Andre B P van Kuilenburg; Adilia Warris; Carlo Marcelis

doi:10.1016/j.jaci.2012.11.006

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

Joyce Geelen, Rolph Pfundt, Judith Meijer, Frans W Verheijen, Andre B P van Kuilenburg, Adilia Warris, Carlo Marcelis

Applied Medicine

Research output: Contribution to journal › Letter › peer-review

4 Citations (Scopus)

Original language	English
Pages (from-to)	222-223
Number of pages	2
Journal	Journal of Allergy and Clinical Immunology
Volume	132
Issue number	1
Early online date	20 Dec 2012
DOIs	https://doi.org/10.1016/j.jaci.2012.11.006
Publication status	Published - Jul 2013

Keywords

Letter

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Cite this

Geelen, J., Pfundt, R., Meijer, J., Verheijen, F. W., van Kuilenburg, A. B. P., Warris, A., & Marcelis, C. (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. https://doi.org/10.1016/j.jaci.2012.11.006

Geelen, J, Pfundt, R, Meijer, J, Verheijen, FW, van Kuilenburg, ABP, Warris, A & Marcelis, C 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, vol. 132, no. 1, pp. 222-223. https://doi.org/10.1016/j.jaci.2012.11.006

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