The nemaline myopathy-causing E117K mutation in β-tropomyosin reduces thin filament activation
Author:
Publisher
Elsevier BV
Subject
Molecular Biology,Biochemistry,Biophysics
Reference46 articles.
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3. The Primary Causes of Muscle Dysfunction Associated with the Point Mutations in Tpm3.12; Conformational Analysis of Mutant Proteins as a Tool for Classification of Myopathies;International Journal of Molecular Sciences;2018-12-10
4. Hereditary Myopathies;Muscle Cell and Tissue - Current Status of Research Field;2018-10-10
5. The primary cause of muscle disfunction associated with substitutions E240K and R244G in tropomyosin is aberrant behavior of tropomyosin and response of actin and myosin during ATPase cycle;Archives of Biochemistry and Biophysics;2018-04
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