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Familial Aicardi–Goutières syndrome due to SAMHD1 mutations is associated with chronic arthropathy and contractures

✍ Scribed by Russell C. Dale; Hannah Gornall; Davinder Singh-Grewal; Melanie Alcausin; Gillian I. Rice; Yanick J. Crow


Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
119 KB
Volume
152A
Category
Article
ISSN
1552-4825

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