Tropomyosins in skeletal muscle diseases.

@article{Kee2008TropomyosinsIS,
  title={Tropomyosins in skeletal muscle diseases.},
  author={Anthony Kee and Edna C Hardeman},
  journal={Advances in experimental medicine and biology},
  year={2008},
  volume={644},
  pages={143-57}
}
A number of congenital muscle diseases and disorders are caused by mutations in genes that encode the proteins present in or associated with the thin filaments of the muscle sarcomere. These genes include alpha-skeletal actin (ACTA1), beta-tropomyosin (TPM2), alpha-tropomyosin slow (TPM3), nebulin (NEB), troponin I fast (TNNI2), troponin T slow (TNNT1), troponin T fast (TNNT3) and cofilin (CFL2). Mutations in two of the four tropomyosin (Tm) genes, TPM2 and TPM3, result in at least three… CONTINUE READING

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Journal of Muscle Research and Cell Motility • 2016
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