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Producer: 20200518
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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. [electronic resource] by
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- Nagai, Shizuyo
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- Doi, Hiraku
- Nomura, Anryu
- Masue, Michiya
- Nishibori, Hironori
- Yoshizawa, Akihiko
- Okamoto, Shinya
- Doi, Ryuichiro
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Producer: 20110204
In:
The Journal of clinical endocrinology and metabolism vol. 96
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