Genetic determinants of urolithiasis
Author:
Publisher
Springer Science and Business Media LLC
Subject
Nephrology
Link
http://www.nature.com/articles/nrneph.2011.211.pdf
Reference129 articles.
1. Clubbe, W. H. Hereditariness of stone. Lancet 99, 204 (1872).
2. Clubbe, W. H. Family disposition to urinary concretions. Lancet 104, 823 (1874).
3. Thorleifsson, G. et al. Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral density. Nat. Genet. 41, 926–930 (2009).
4. Weber, S. et al. Novel paracellin-1 mutations in 25 families with familial hypomagnesemia with hypercalciuria and nephrocalcinosis. J. Am. Soc. Nephrol. 12, 1872–1881 (2001).
5. Konrad, M. et al. Mutations in the tight-junction gene claudin 19 (CLDN19) are associated with renal magnesium wasting, renal failure, and severe ocular involvement. Am. J. Hum. Genet. 79, 949–957 (2006).
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