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).
Чикаго стиль цитування (17-те видання)Lloyd, SE, S. Pearce, W. Günther, H. Kawaguchi, T. Igarashi, T. Jentsch, та 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.
Стиль цитування MLA (9-ме видання)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.