Myopathy-causing mutation R91P in the TPM3 gene drastically impairs structural and functional properties of slow skeletal muscle tropomyosin γβ-heterodimer. - Gonchar AD; Koubassova NA; Kopylova GV; Kochurova AM; Nefedova VV; Yampolskaya DS; Shchepkin DV; Bershitsky SY; Tsaturyan AK; Matyushenko AM; Levitsky DI (Archives of biochemistry and biophysics, 2024)