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Molecular and clinical analysis of Japanese patients with persistent congenital hyperinsulinism: predominance of paternally inherited monoallelic mutations in the KATP channel genes |
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| Authors: | Yorifuji Tohru Kawakita Rie Nagai Shizuyo Sugimine Akinori Doi Hiraku Nomura Anryu Masue Michiya Nishibori Hironori Yoshizawa Akihiko Okamoto Shinya Doi Ryuichiro Uemoto Shinji Nagasaka Hironori |
| Affiliation: | Department of Pediatric Endocrinology and Metabolism, Osaka City General Hospital, Miyakojima, Osaka, Japan. t-yorifuji@hospital.city.osaka.jp |
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| 本文献已被 PubMed 等数据库收录！ | |