Hallmark Features of the Tropomyosin Regulatory Function in Several Variants of Congenital Myopathy
Author:
Publisher
Pleiades Publishing Ltd
Subject
Physiology,Biochemistry,Ecology, Evolution, Behavior and Systematics
Link
https://link.springer.com/content/pdf/10.1134/S0022093021030133.pdf
Reference85 articles.
1. Matyushenko AM, Levitsky DI (2020) Molecular Mechanisms of Pathologies of Skeletal and Cardiac Muscles Caused by Point Mutations in the Tropomyosin Genes. Biochemistry (Mosc) 85(Suppl 1):S20-S33. https://doi.org/10.1134/S0006297920140023
2. Moraczewska J (2020) Thin filament dysfunctions caused by mutations in tropomyosin Tpm3.12 and Tpm1.1. J Muscle Res Cell Motil 41(1):39-53. https://doi.org/10.1007/s10974-019-09532-y
3. Jungbluth H, Treves S, Zorzato F, Sarkozy A, Ochala J, Sewry C, Phadke R, Gautel M, Muntoni F (2018) Congenital myopathies: disorders of excitation-contraction coupling and muscle contraction. Nat Rev Neurol 14:151–167. https://doi.org/10.1038/nrneurol.2017.191
4. Ravenscroft G, Bryson-Richardson RJ, Nowak KJ, Laing NG (2018) Recent advances in understanding congenital myopathies. F1000Res 7:F1000 Faculty Rev-1921. https://doi.org/10.12688/f1000research.16422.1
5. Gonorazky HD, Bonnemann CG, Dowling JJ (2018) The genetics of congenital myopathies. Handb Clin Neurol 148:549–564. https://doi.org/10.1016/B978-0-444-64076-5.00036-3
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