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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Auteurs principaux: 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
Format: Artigo
Langue:Inglês
Publié: 2009
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Article
Accès en ligne: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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