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Phenotypic variability in patients with ADA2 deficiency due to identical homozygous R169Q mutations
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,Volume:
13
Language:
english
Journal:
Pediatric Rheumatology
DOI:
10.1186/1546-0096-13-s1-o7
Date:
December, 2015
File:
PDF, 268 KB
english, 2015