A novel mutation in the human mineralocorticoid receptor gene in a Japanese family with autosomal-dominant pseudohypoaldosteronism type 1.
| Autor: | Yoshimi Nishizaki1, Makoto Hiura2, Hidetoshi Sato1, Yohei Ogawa1, Akihiko Saitoh1, Keisuke Nagasaki1 nagasaki@med.niigata-u.ac.jp |
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| Zdroj: | Clinical Pediatric Endocrinology. Oct2016, Vol. 25 Issue 4, p135-138. 4p. |
| Databáze: | Academic Search Ultimate |
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