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J-GLOBAL ID：201902218979044482   Reference number：19A0104844

KCNJ3 N496H A Rare Variant in Japanese as a Cause of Susceptible Gene for Ventricular Fibrillation in Overlap Syndromes between LQT and CPVT

日本人におけるKCNJ3 N496H変異はLQTとCPTVのオーバーラップ症候群における心室細動の易患性遺伝子としては稀である

Author (20)： AIBA Takeshi (National Cerebral and Cardiovascular Center, JPN) ,  OHNO Seiko (Shiga Univ. Medical Sci.) ,  ONO Mayuko (Shiga Univ. Medical Sci.) ,  SHIGEMIZU Daichi (Tokyo Medical and Dental Univ.) ,  TOYODA Futoshi (Shiga Univ. Medical Sci.) ,  MIAKE Junichiro (Tottori Univ.) ,  HAGIWARA Akiko (Kanagawa Children’s Medical Center) ,  SHINOHARA Toru (Kinki Univ.) ,  OKUMURA Satoshi (Konan Kosei Hospital) ,  TODA Tatsushi (Kobe Univ.) ,  SATAKE Wataru (Kobe Univ.) ,  TSUNODA Tatsuhiko (RIKEN) ,  SHIMAMOTO Keiko (National Cerebral and Cardiovascular Center, JPN) ,  SEKINE Akihiko (National Cerebral and Cardiovascular Center, JPN) ,  TAKAHASHI Atsushi (National Cerebral and Cardiovascular Center, JPN) ,  MIYAMOTO Yoshihiro (National Cerebral and Cardiovascular Center, JPN) ,  TANAKA Toshihiro (Tokyo Medical and Dental Univ.) ,  KUSANO Kengo (National Cerebral and Cardiovascular Center, JPN) ,  HORIE Minoru (Shiga Univ. Medical Sci.) ,  SHIMIZU Wataru (Nippon Medical School)
Material： 日本不整脈心電学会学術大会プログラム・抄録集(Web)  (日本不整脈心電学会学術大会抄録集(Web))
Volume： 64th  Page： ROMBUNNO.GS3-2 (WEB ONLY)  Publication year： 2017 
JST Material Number： U1484A  Document type： Proceedings
Article type： 会議録記事  Country of issue： Japan (JPN)  Language： ENGLISH (EN)

Thesaurus term： human ,...
Semi thesaurus term： *KCNJ3遺伝子 ,...

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JST classification (3)： Basic medicine on cardiovascular system  (GJ01020K) ,  Congenital diseases,deformities in general.  (GD03010V) ,  Molecular genetics in general  (EC02010J)

Terms in the title (5)： 日本人 ,  変異 ,  オーバーラップ症候群 ,  心室細動 ,  遺伝子