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Functional investigation of troponin with the homozygous HCM mutation, TNNT2 K280N, obtained from an explanted heart

Functional investigation of troponin with the homozygous HCM mutation, TNNT2 K280N, obtained from an explanted heart

书目详细资料
Main Authors: Bayliss, C, Messer, A, Leung, M, Ward, D, Van Der Velden, J, Poggesi, C, Redwood, C, Marston, S
格式: Conference item
出版: 2012
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  • Low expression of the K280N TNNT2 mutation is sufficient to increase basal myofilament activation in human hypertrophy cardiomyopathy
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  • Mutations in troponin T associated with Hypertrophic Cardiomyopathy increase Ca2+-sensitivity and suppress the modulation of Ca2+-sensitivity by troponin I phosphorylation
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