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Familial cases of pseudohypoaldosteronism type II harboring a novel mutation in the Cullin 3 gene.

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Bibliographic Details
Title:	Familial cases of pseudohypoaldosteronism type II harboring a novel mutation in the Cullin 3 gene.
Authors:	Nakano, Kiyoshi¹ (AUTHOR), Kubota, Yasuo^1,2 (AUTHOR) yasuo-k@dj9.so-net.ne.jp, Mori, Takayuki^1,2 (AUTHOR), Chiga, Motoko³ (AUTHOR), Mori, Takayasu³ (AUTHOR), Sonoda, Shyunya¹ (AUTHOR), Ueda, Daisuke¹ (AUTHOR), Asakura, Isao¹ (AUTHOR), Ikegaya, Takeshi¹ (AUTHOR), Kagawa, Jiro¹ (AUTHOR), Uchida, Shinichi³ (AUTHOR), Kubota, Akira¹ (AUTHOR)
Source:	Nephrology. Nov2020, Vol. 25 Issue 11, p818-821. 4p.
Database:	Academic Search Ultimate
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