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 journalLetter

3 Citations (Scopus)
Original languageEnglish
Pages (from-to)222-223
Number of pages2
JournalJournal of Allergy and Clinical Immunology
Volume132
Issue number1
Early online date20 Dec 2012
DOIs
Publication statusPublished - Jul 2013

Keywords

  • Letter

Cite this

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; Verheijen, Frans W; van Kuilenburg, Andre B P; Warris, Adilia; Marcelis, Carlo.

In: Journal of Allergy and Clinical Immunology, Vol. 132, No. 1, 07.2013, p. 222-223.

Research output: Contribution to journalLetter

Geelen, Joyce ; Pfundt, Rolph ; Meijer, Judith ; Verheijen, Frans W ; van Kuilenburg, Andre B P ; Warris, Adilia ; Marcelis, Carlo. / Severe phenotype of severe combined immunodeficiency caused by adenosine deaminase deficiency in a patient with a homozygous mutation due to uniparental disomy. In: Journal of Allergy and Clinical Immunology. 2013 ; Vol. 132, No. 1. pp. 222-223.
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AU - Verheijen, Frans W

AU - van Kuilenburg, Andre B P

AU - Warris, Adilia

AU - Marcelis, Carlo

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