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Homozygosity for uromodulin disorders: FJHN and MCKD-type 2.
Kidney Int. 2004 Aug;66(2):558-63. doi: 10.1111/j.1523-1755.2004.00774.x.
Kidney Int. 2004.
PMID: 15253706
Free article.
A novel pattern of mutation in uromodulin disorders: autosomal dominant medullary cystic kidney disease type 2, familial juvenile hyperuricemic nephropathy, and autosomal dominant glomerulocystic kidney disease.
Lens XM, Banet JF, Outeda P, Barrio-Lucía V.
Lens XM, et al. Among authors: banet jf.
Am J Kidney Dis. 2005 Jul;46(1):52-7. doi: 10.1053/j.ajkd.2005.04.003.
Am J Kidney Dis. 2005.
PMID: 15983957
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