VIII  DNAの構造解析・遺伝子発現  5.心臓ナトリウムイオンチャネルコード遺伝子(SCN5A)転写調節領域におけるディプロタイプ解析

NAKATOME MASATO; HAMAJIMA MAKOTO; HIRATA YUKARI; ISOBE ICHIRO; YAMAMOTO TAKUMA; MATOBA RYOJI

Art

J-GLOBAL ID：201002266106045944 Reference number：10A0585936

VIII DNAの構造解析・遺伝子発現 5.心臓ナトリウムイオンチャネルコード遺伝子(SCN5A)転写調節領域におけるディプロタイプ解析

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Material：
Volume： 18 Page： 268-271 Publication year： May. 30, 2010
JST Material Number： L5455A ISSN： 2188-3815 Document type： Article
Article type：短報 Country of issue： Japan (JPN) Language： JAPANESE (JA)

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Cardiovascular system diseases , Molecular genetics in general

Reference (9)：

MORIC-JANISZEWSKA, E. Challenges of diagnosis of long-QT syndrome in children. Pacing Clin Electrophysiol. 2007, 30, 1168-1170
HORIE, M. Disorders of cardiac repolarization-long QT and short QT syndromes-. Circ J. 2007, Suppl A, A50-A53
ANTZELEVITCH, C. Brugada syndrome : report of the second consensus conference. Heart Rhythm. 2005, 2, 429-440
CLANCY, CE. Mutation-specific effects of lidocaine in Brugada syndrome. Int J Cardiol. 2007, 121, 249-252
KOOPMANN, TT. Exclusion of multiple candidate genes and large genomic rearrangements in SCN5A in a Dutch Brugada syndrome cohort. Heart Rhythm. 2007, 4, 752-755

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