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De Novo Asp219Val Mutation in Cardiac Tropomyosin Associated with Hypertrophic Cardiomyopathy.
Int J Mol Sci. 2022 Dec 20;24(1):18. doi: 10.3390/ijms24010018.
Int J Mol Sci. 2022.
PMID: 36613463
Free PMC article.
Effects of myopathy-causing mutations R91P and R245G in the TPM3 gene on structural and functional properties of slow skeletal muscle tropomyosin.
Gonchar AD, Kopylova GV, Kochurova AM, Berg VY, Shchepkin DV, Koubasova NA, Tsaturyan AK, Kleymenov SY, Matyushenko AM, Levitsky DI.
Gonchar AD, et al. Among authors: koubasova na.
Biochem Biophys Res Commun. 2021 Jan 1;534:8-13. doi: 10.1016/j.bbrc.2020.11.103. Epub 2020 Dec 8.
Biochem Biophys Res Commun. 2021.
PMID: 33307294
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