Art

J-GLOBAL ID：200902110714803176   Reference number：95A0339349

SCN5A Mutations Associated with an Inherited Cardiac Arrhythmia, Long QT Syndrome.

SCN5A突然変異は遺伝性心臓不整脈,QT延長症候群と関連している

Author (9)： WANG Q (Univ. Utah Health Sciences Center, Utah) ,  SHEN J (Univ. Utah Health Sciences Center, Utah) ,  SPLAWSKI I (Univ. Utah Health Sciences Center, Utah) ,  ATKINSON D (Univ. Utah Health Sciences Center, Utah) ,  LI Z (Univ. Utah Health Sciences Center, Utah) ,  ROBINSON J L (Univ. Rochester Medical Center, New York) ,  MOSS A J (Univ. Rochester Medical Center, New York) ,  TOWBIN J A (Baylor Coll. Medicine, Texas) ,  KEATING M T (Univ. Utah Health Sciences Center, Utah)
Material： Cell (Cambridge, Mass.)  (Cell (Camb. Mass.))
Volume： 80  Issue： 5  Page： 805-811  Publication year： Mar. 10, 1995 
JST Material Number： A0707B  ISSN： 0092-8674  Document type： Article
Article type： 原著論文  Country of issue： United States (USA)  Language： ENGLISH (EN)

Thesaurus term： gene ,...
Semi thesaurus term： linkage(genetics) ,...

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JST classification (3)： Molecular genetics in general  (EC02010J) ,  Congenital diseases,deformities in general.  (GD03010V) ,  Cardiovascular system diseases  (GJ03000C)

Terms in the title (5)： SCN5A ,  突然変異 ,  遺伝 ,  心臓不整脈 ,  QT延長症候群