NewslettersHepatic Cell NewsMuscle Cell NewsNeural Cell NewsOrganoid News Myopathy-Causing Mutation R91P in the TPM3 Gene Drastically Impairs Structural and Functional Properties of Slow Skeletal Muscle Tropomyosin γβ-Heterodimer By Noshin Noorjahan - January 8, 2024 0 The authors investigated the influence of the R91P mutation in the γ-chain on the properties of the γβ-tropomyosin heterodimer. [Archives of Biochemistry and Biophysics] AbstractGraphical Abstract