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See Latest ArticlesGenotype-Phenotype Aspects of Type 2 Long QT Syndrome
JACC - Journal of the American College of Cardiology, 11/25/09
Shimizu W et al. – The KCNH2 missense mutations located in the transmembrane S5–loop–S6 region are associated with the greatest risk.
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Today in Basic Science/Genetics...keeping you current
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NKX2.5 mutations in patients with non-syndromic congenital heart disease
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