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

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Title: Familial cases of pseudohypoaldosteronism type II harboring a novel mutation in the Cullin 3 gene.
Authors: Nakano, Kiyoshi1 (AUTHOR), Kubota, Yasuo1,2 (AUTHOR) yasuo-k@dj9.so-net.ne.jp, Mori, Takayuki1,2 (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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  Data: Familial cases of pseudohypoaldosteronism type II harboring a novel mutation in the Cullin 3 gene.
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  Data: <searchLink fieldCode="JN" term="%22Nephrology%22">Nephrology</searchLink>. Nov2020, Vol. 25 Issue 11, p818-821. 4p.
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        Value: 10.1111/nep.13752
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        Text: English
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              Text: Nov2020
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