We studied purine metabolism in gouty patients from three categories: primary gout, familial juvenile hyperuricaemic nephropathy (FJHN) and partial HPRT deficiency.
CITATION STYLE
Grahame, R., Simmonds, H. A., McBride, M. B., & Marsh, F. P. (1998). How should we treat tophaceous gout in patients with allopurinol hypersensitivity? In Advances in Experimental Medicine and Biology (Vol. 431, pp. 19–23). Springer New York LLC. https://doi.org/10.1007/978-1-4615-5381-6_4
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