Congenital nephrogenic diabetes insipidus with end-stage renal disease
Hyun Ho Ryu, Jong Hoon Chung, Byung Chul Shin, Hyun Lee Kim
Korean J Intern Med. 2015;30(2):259-261. Published online 2015 Feb 27 DOI: https://doi.org/10.3904/kjim.2015.30.2.259
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