FRET-based analysis of the cardiac troponin T linker region reveals the structural basis of the hypertrophic cardiomyopathy-causing Δ160E mutation

Author:

Abdullah Salwa,Lynn Melissa L.ORCID,McConnell Mark T.,Klass Matthew M.,Baldo Anthony P.ORCID,Schwartz Steven D.,Tardiff Jil C.

Funder

HHS | NIH | National Heart, Lung, and Blood Institute

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference64 articles.

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3. Molecular genetics and pathogenesis of cardiomyopathy;Kimura;J. Hum. Genet,2015

4. Results of clinical genetic testing of 2,912 probands with hypertrophic cardiomyopathy: expanded panels offer limited additional sensitivity;Alfares;Genet. Med,2015

5. Calcium regulation of thin filament movement in an in vitro motility assay;Homsher;Biophys. J,1996

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