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

5 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

Access to Document

10.1016/j.jaci.2012.11.006Licence: Unspecified

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

@article{733b24a344aa43ea8f716e5c8bfbfc3c,

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

keywords = "Letter",

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",

year = "2013",

month = jul,

doi = "10.1016/j.jaci.2012.11.006",

language = "English",

volume = "132",

pages = "222--223",

journal = "Journal of Allergy and Clinical Immunology",

issn = "0091-6749",

publisher = "Elsevier Inc.",

number = "1",

}

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 - 2013/7

Y1 - 2013/7

KW - Letter

U2 - 10.1016/j.jaci.2012.11.006

DO - 10.1016/j.jaci.2012.11.006

M3 - Letter

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 -