Author:
Igarashi Takashi,Inatomi Jun,Ohara Toshio,Kuwahara Takashi,Shimadzu Mitsunobu,Thakker Rajesh V.
Reference22 articles.
1. A common molecular basis for three inherited kidney stone diseases;Lloyd;Nature,1996
2. Idiopathic low molecular weight proteinuria associated with hypercalciuric nephrocalcinosis in Japanese children is due to the mutations of renal chloride channel (CLCN5);Lloyd;J Clin Invest,1997
3. Characterization of renal chloride channel, CLCN5, mutations in hypercalciuric nephrocalcinosis (kidney stones) disorders;Lloyd;Hum Mol Genet,1997
4. Dent's disease: A familial proximal renal tubular syndrome with low-molecular-weight proteinuria, hypercalciuria, nephrocalcinosis, metabolic bone disease, progressive renal failure and a marked male predominance;Wrong;Q J Med,1994
5. Hypercalciuria and nephrocalcinosis in patients with idiopathic low molecular weight proteinuria in Japan: Is the disease identical to Dent's disease?;Igarashi;Nephron,1995
Cited by
52 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献