文献

J-GLOBAL ID：201902220328139668   整理番号：19S1537892

A CACNB4 mutation shows that altered Cav2.1 function may be a genetic modifier of severe myoclonic epilepsy in infancy

著者 (9件)： Ohmori, Iori (Department of Physiology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University) ,  Nishiki, Teiichi (Department of Physiology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University) ,  Tomizawa, Kazuhito (Department of Physiology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University) ,  Matsui, Hideki (Department of Physiology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University) ,  Ouchida, Mamoru (Department of Molecular Genetics, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University) ,  Miki, Takafumi (Department of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto University) ,  Kiyonaka, Shigeki (Department of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto University) ,  Mori, Yasuo (Department of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto University) ,  Mimaki, Nobuyoshi (Pediatrics, Kurashiki Medical Center)
資料名： Neurobiology of Disease
巻： 32  号： 3  ページ： 349-354  発行年： 2008年 
JST資料番号： SCOPUS  ISSN： 0969-9961  CODEN： NUDIE 
発行国： アメリカ (USA)  言語： 英語 (EN)

タイトルに関連する用語 (1件)： Be