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, et al. Arch Biochem Biophys. 2024 Feb; 752:109881. Epub 2024 Jan 6.