A case of familial hypocalciuric hypercalcemia type 1 due to CASR p.Pro55Leu mutation.

Autor: Sumida, Akira1, Iizuka, Katsumi1,2,3 katsumi.iizuka@fujita-hu.ac.jp, Kato, Takehiro1, Liu, Yanyan1, Kubota, Sodai1,4, Kubota-Okamoto, Saki1,4, Sakurai, Teruaki1, Imaizumi, Toshinori1, Takahashi, Yoshihiro1, Mizuno, Masami1, Takao, Ken1, Hirota, Takuo1, Suwa, Tetsuya1, Horikawa, Yukio1, Yamamoto, Mayumi5, Seino, Yusuke6, Suzuki, Atsushi6, Yabe, Daisuke1,3,7,8
Zdroj: BMC Endocrine Disorders. 6/22/2022, Vol. 22 Issue 1, p1-5. 5p.
Databáze: Academic Search Ultimate
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