Lloyd, S., Pearce, S., Günther, W., Kawaguchi, H., Igarashi, T., Jentsch, T., & Thakker, R. (1997). Idiopathic low molecular weight proteinuria associated with hypercalciuric nephrocalcinosis in Japanese children is due to mutations of the renal chloride channel (CLCN5).
Citace podle Chicago (17th ed.)Lloyd, SE, S. Pearce, W. Günther, H. Kawaguchi, T. Igarashi, T. Jentsch, a R. Thakker. Idiopathic Low Molecular Weight Proteinuria Associated with Hypercalciuric Nephrocalcinosis in Japanese Children Is Due to Mutations of the Renal Chloride Channel (CLCN5). 1997.
Citace podle MLA (9th ed.)Lloyd, SE, et al. Idiopathic Low Molecular Weight Proteinuria Associated with Hypercalciuric Nephrocalcinosis in Japanese Children Is Due to Mutations of the Renal Chloride Channel (CLCN5). 1997.