APA-ийн эшлэл(7 дахь хэвлэлт)

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-гийн эшлэл (17 дахь хэвлэлт)

Lloyd, SE, S. Pearce, W. Günther, H. Kawaguchi, T. Igarashi, T. Jentsch, ба 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.

MLA -ийн эшлэл (9 дэх хэвлэлт)

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.

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