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).
Trích dẫn kiểu Chicago (xuất bản lần thứ 7)Lloyd, SE, S. Pearce, W. Günther, H. Kawaguchi, T. Igarashi, T. Jentsch, và 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.
Trích dẫn kiểu MLA (xuất bản lần thứ 9)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.