Phenotypic variability in patients with ADA2 deficiency due to identical homozygous R169Q mutations. Issue 1 (December 2015)

• Record Type: Journal Article
• Authors: Van Montfrans, J; Hartman, E; Braun, K; Hennekam, F; Hak, A; Nederkoorn, P; Westendorp, W; Bredius, R; Kollen, W; Scholvinck, E; Legger, G; Meyts, I; Liston, A; Lichtenbelt, K; Giltay, J; Van Haaften, G; De Vries Simons, G; Leavis, H; Nierkens, S; Sanders, C; Van Gijn, M
• Is Part Of: Pediatric rheumatology online journal. Volume 13:Issue 1(2015)
• Page Start: 1
• Page End: 2
• Publication Date: 2015-12
• Subjects: Pediatric rheumatology -- Periodicals; Rheumatism in children -- Periodicals; 618.92723
• DOI: 10.1186/1546-0096-13-S1-O7
• Languages: English
• ISSNs: 1546-0096