Genotype-Phenotype Aspects of Type-2 Long-QT Syndrome

OBJECTIVES: To investigate the effect of location, coding type, and topology of KCNH2(hERG) mutations on clinical phenotype in Type-2 long-QT syndrome. BACKGROUNDS: Previous studies were limited by population size in their ability to examine phenotypic effect of location, type and topology. METHODS:...

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Detalhes bibliográficos
Main Authors: Shimizu, Wataru, Moss, Arthur J., Wilde, Arthur A.M., Towbin, Jeffrey A., Ackerman, Michael J., January, Craig T., Tester, David J., Zareba, Wojciech, Robinson, Jennifer L., Qi, Ming, Michael Vincent, G., Kaufman, Elizabeth S., Hofman, Nynke, Noda, Takashi, Kamakura, Shiro, Miyamoto, Yoshihiro, Shah, Samit, Amin, Vinit, Goldenberg, Ilan, Andrews, Mark L, McNitt, Scott
Formato: Artigo
Idioma:Inglês
Publicado em: 2009
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2808400/
https://ncbi.nlm.nih.gov/pubmed/19926013
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jacc.2009.08.028
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