KCNQ1 mutations in patients with a family history of lethal cardiac arrhythmias and sudden death

Long QT syndrome (LQTS) is the prototype of the cardiac ion channelopathies which cause syncope and sudden death. LQT1, due to mutations of KCNQ1 (KVLQT1), is the most common form. This study describes the genotype–phenotype characteristics in 10 families with mutations of KCNQ1, including 5 novel m...

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Detalhes bibliográficos
Main Authors: Chen, S, Zhang, L, Bryant, RM, Vincent, GM, Flippin, M, Lee, JC, Brown, E, Zimmerman, F, Rozich, R, Szafranski, P, Oberti, C, Sterba, R, Marangi, D, Tchou, PJ, Chung, MK, Wang, Q
Formato: Artigo
Idioma:Inglês
Publicado em: 2003
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1579805/
https://ncbi.nlm.nih.gov/pubmed/12702160
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