Genome-wide study of familial juvenile hyperuricaemic (gouty) nephropathy (FJHN) indicates a new locus, FJHN3, linked to chromosome 2p22.1-p21

Genome-wide study of familial juvenile hyperuricaemic (gouty) nephropathy (FJHN) indicates a new locus, FJHN3, linked to chromosome 2p22.1-p21

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Familial juvenile hyperuricaemic (gouty) nephropathy (FJHN), is an autosomal dominant disease associated with a reduced fractional excretion of urate, and progressive renal failure. FJHN is genetically heterogeneous and due to mutations of three genes: uromodulin (UMOD), renin (REN) and hepatocyte n...

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Main Authors: Piret, SE, Danoy, P, Dahan, K, Reed, A, Pryce, K, Wong, W, Torres, R, Puig, J, Müller, T, Kotanko, P, Lhotta, K, Devuyst, O, Brown, M, Thakker, R
Format: Journal article
Language:English
Published: 2011

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