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:https://doi.org/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

Research output: Contribution to journal › Comment/Letter to the editor › Academic

4 Citations (Scopus)

Original language	English
Pages (from-to)	222-223
Journal	Journal of allergy and clinical immunology
Volume	132
Issue number	1
DOIs	https://doi.org/10.1016/j.jaci.2012.11.006
Publication status	Published - 2013

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https://doi.org/10.1016/j.jaci.2012.11.006

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

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

author = "Joyce Geelen and Rolph Pfundt and Judith Meijer and Verheijen, {Frans W.} and {van Kuilenburg}, {Andre B. P.} and Adilia Warris and Carlo Marcelis",

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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

Severe phenotype of severe combined immunodeficiency caused by adenosine deaminase deficiency in a patient with a homozygous mutation due to uniparental disomy. / Geelen, Joyce; Pfundt, Rolph; Meijer, Judith et al.
In: Journal of allergy and clinical immunology, Vol. 132, No. 1, 2013, p. 222-223.

Research output: Contribution to journal › Comment/Letter to the editor › Academic

TY - JOUR

T1 - Severe phenotype of severe combined immunodeficiency caused by adenosine deaminase deficiency in a patient with a homozygous mutation due to uniparental disomy

AU - Geelen, Joyce

AU - Pfundt, Rolph

AU - Meijer, Judith

AU - Verheijen, Frans W.

AU - van Kuilenburg, Andre B. P.

AU - Warris, Adilia

AU - Marcelis, Carlo

PY - 2013

Y1 - 2013

U2 - https://doi.org/10.1016/j.jaci.2012.11.006

DO - https://doi.org/10.1016/j.jaci.2012.11.006

M3 - Comment/Letter to the editor

C2 - 23260757

SN - 0091-6749

VL - 132

SP - 222

EP - 223

JO - Journal of allergy and clinical immunology

JF - Journal of allergy and clinical immunology

IS - 1

ER -