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Start Over You searched for: Author "Nowak KJ" Remove constraint Author: "Nowak KJ" Topic muscle fibers, skeletal Remove constraint Topic: muscle fibers, skeletal
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1. TPM3 deletions cause a hypercontractile congenital muscle stiffness phenotype.

2. K7del is a common TPM2 gene mutation associated with nemaline myopathy and raised myofibre calcium sensitivity.

3. Novel application of flow cytometry: determination of muscle fiber types and protein levels in whole murine skeletal muscles and heart.

4. Dissociated flexor digitorum brevis myofiber culture system--a more mature muscle culture system.

5. Fatal hypertrophic cardiomyopathy and nemaline myopathy associated with ACTA1 K336E mutation

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