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Article

Alterations of uromodulin biology: a common denominator of the genetically heterogeneous FJHN/MCKD syndrome

2 Aug 2006

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Share to Ion Transport and Channel Regulation
Share to Kidney Stones and Urolithiasis Treatments
Share to Pediatric Urology and Nephrology Studies

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 16883323
DOI: 10.1038/sj.ki.5001728

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Alterations of uromodulin biology: a common denominator of the genetically heterogeneous FJHN/MCKD syndromePMID 16883323Read ↗

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Allelic and Gene Dosage Effects Involving Uromodulin Aggregates Drive Autosomal Dominant Tubulointerstitial Kidney DiseaseSemantic proximity Read ↗

Genome-wide studies reveal factors associated with circulating uromodulin and its relationships to complex diseasesSemantic proximity Read ↗

The Uromodulin C744G mutation causes MCKD2 and FJHN in children and adults and may be due to a possible founder effect.Semantic proximity Read ↗

Genetic kidney disease: Uromodulin in ER stress and apoptosis.Semantic proximity Read ↗

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