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

✍ Scribed by Geelen, Joyce; Pfundt, Rolph; Meijer, Judith; Verheijen, Frans W.; van Kuilenburg, Andre B.P.; Warris, Adilia; Marcelis, Carlo

• Book ID: 121479276
• Publisher: Elsevier Science
• Year: 2013
• Tongue: English
• Weight: 76 KB
• Volume: 132
• Category: Article
• ISSN: 1097-6825
• DOI: 10.1016/j.jaci.2012.11.006