Familial nephropathy associated with hyperuricemia in Spain: Our experience with 3 families harbouring a UMOD mutation

Nucleosides, Nucleotides and Nucleic Acids

Volumn 25, Issue 9-11, 2006, Pages 1295-1300

  Puig, J G ^a   Prior, C ^a   Martinez Ara J ^a   Torres, Rosa Jiménez ^a  

^a HOSPITAL UNIVERSITARIO LA PAZ   (Spain)

Author keywords

Renal insufficiency; Uric acid; Uromodulin

Indexed keywords

ALLOPURINOL; TAMM HORSFALL GLYCOPROTEIN;

ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOME 16P; CLINICAL FEATURE; DISEASE ASSOCIATION; FAMILIAL DISEASE; GENE; GENETIC LINKAGE; GOUT; HUMAN; HYPERTENSION; HYPERURICEMIA; KIDNEY DISEASE; KIDNEY FAILURE; KIDNEY SIZE; PATHOPHYSIOLOGY; POINT MUTATION; UMOD GENE;

ADULT; DNA MUTATIONAL ANALYSIS; EXONS; FAMILY HEALTH; FEMALE; HUMANS; HYPERURICEMIA; KIDNEY; KIDNEY DISEASES; LINKAGE (GENETICS); MALE; MIDDLE AGED; MUCOPROTEINS; MUTATION; RENAL INSUFFICIENCY; URIC ACID;

EID: 33750492977     PISSN: 15257770     EISSN: 15322335     Source Type: Journal    
DOI: 10.1080/15257770600894766     Document Type: Article

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