Phenotypic variability in patients with ADA2 deficiency due...

Pediatric Rheumatology 2015 / 12 Vol. 13; Iss. 1 Suppleme

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,
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Volume:
13
Language:
english
Journal:
Pediatric Rheumatology
DOI:
10.1186/1546-0096-13-s1-o7
Date:
December, 2015
File:
PDF, 268 KB
english, 2015
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