(Q33718171)
Statements
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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 (English)
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Shinji Uemoto
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Tohru Yorifuji
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Rie Kawakita
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Shizuyo Nagai
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Akinori Sugimine
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Hiraku Doi
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Anryu Nomura
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Michiya Masue
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Hironori Nishibori
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Akihiko Yoshizawa
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Shinya Okamoto
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Ryuichiro Doi
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Hironori Nagasaka
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13 October 2010
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96
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E141-5
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Identifiers
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