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Abnormal heart rate regulation in murine hearts with familial hypertrophic cardiomyopathy-related cardiac troponin T mutations

Mutations in cardiac troponin T (cTnT), Δ160E and R92Q, have been linked to familial hypertrophic cardiomyopathy (FHC), and some studies have indicated that these mutations can lead to a high incidence of sudden cardiac death in the relative absence of significant ventricular hypertrophy. Alteration...

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Autors principals: Jimenez, Jesus, Tardiff, Jil C.
Format: Artigo
Idioma:Inglês
Publicat: American Physiological Society 2011
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3044052/
https://ncbi.nlm.nih.gov/pubmed/21131475
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/ajpheart.00247.2010
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