A complete deficiency of Hyaluronoglucosaminidase 1 (HYAL1) presenting as familial juvenile idiopathic arthritis
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/s10545-011-9343-3
Reference17 articles.
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4. International FMF Consortium (1997) Ancient missense mutations in a new member of the RoRet gene family are likely to cause familial Mediterranean fever. Cell 90(4):797–807
5. Natowicz MR, Short MP, Wang Y et al. (1996) Clinical and biochemical manifestations of hyaluronidase deficiency. N Engl J Med 335(14):1029–1033
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