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Article

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

The Journal of allergy and clinical immunology - 1 Jul 2013

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

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Share to Adenosine Deaminase
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Share to Chromosomes, Human, Pair 20

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Identifiers

PMID: 23260757
DOI: 10.1016/j.jaci.2012.11.006

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