Mutations in PRRT2 responsible for paroxysmal kinesigenic dyskinesias also cause benign familial infantile convulsions
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概要
著者
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Yoshiura Koh-ichiro
長崎大学 医歯薬学総合研究科人類遺伝学
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Yoshiura Koh‐ichiro
Jst‐sorst Kawaguchi Jpn
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Kinoshita Akira
長崎大学 医歯薬学研究科人類遺伝学
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Yoshimura Shuichiro
長崎大学 医歯薬学総合研究科人類遺伝学
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Yoshiura Koh-ichiro
Department Of Human Genetics Nagasaki University Graduate School Of Biomedical Sciences
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Kinoshita Akira
Department Of Human Genetics Nagasaki University Graduate School Of Biomedical Sciences
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Ono Shinji
Department Of Psychiatry Nagasaki University Hospital
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- A type of familial cleft of the soft palate maps to 2p24.2–p24.1 or 2p21–p12
- Mutations in PRRT2 responsible for paroxysmal kinesigenic dyskinesias also cause benign familial infantile convulsions
- Mutations in PRRT2 responsible for paroxysmal kinesigenic dyskinesias also cause benign familial infantile convulsions
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