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UROMODULIN mutations cause familial juvenile hyperuricemic nephropathy.
Turner, J J O; Stacey, J M; Harding, B; Kotanko, P; Lhotta, K; Puig, J G; Roberts, I; Torres, R J; Thakker, R V.
Affiliation
  • Turner JJ; Molecular Endocrinology Group, Nuffield Department of Medicine, Botnar Research Centre, University of Oxford, Nuffield Orthopaedic Centre, Oxford, OX3 7LD, United Kingdom.
J Clin Endocrinol Metab ; 88(3): 1398-401, 2003 Mar.
Article in En | MEDLINE | ID: mdl-12629136
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Collection: 01-internacional Database: MEDLINE Main subject: Hyperuricemia / Kidney Diseases / Mucoproteins / Mutation Limits: Humans Language: En Journal: J Clin Endocrinol Metab Year: 2003 Document type: Article Affiliation country: Reino Unido
Search on Google
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PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Hyperuricemia / Kidney Diseases / Mucoproteins / Mutation Limits: Humans Language: En Journal: J Clin Endocrinol Metab Year: 2003 Document type: Article Affiliation country: Reino Unido