MYH7 in cardiomyopathy and skeletal muscle myopathy
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cell Biology,Clinical Biochemistry,Molecular Biology,General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s11010-023-04735-x.pdf
Reference277 articles.
1. Oldfors A (2007) Hereditary myosin myopathies. Neuromuscul Disord 17:355–367. https://doi.org/10.1016/j.nmd.2007.02.008
2. Buvoli M, Hamady M, Leinwand LA, Knight R (2008) Bioinformatics assessment of β-myosin mutations reveals myosin’s high sensitivity to mutations. Trends Cardiovasc Med 18:141–149. https://doi.org/10.1016/j.tcm.2008.04.001
3. Jaenicke T, Diederich KW, Haas W, Schleich J, Lichter P, Pfordt M, Bach A, Vosberg H-P (1990) The complete sequence of the human β-myosin heavy chain gene and a comparative analysis of its product. Genomics 8:194–206. https://doi.org/10.1016/0888-7543(90)90272-v
4. Yamauchi-Takihara K, Sole MJ, Liew J, Ing D, Liew C-C (1989) Characterization of human cardiac myosin heavy chain genes. Proc Natl Acad Sci 86:3504–3508. https://doi.org/10.1073/pnas.86.10.3504
5. Geisterfer-Lowrance AA, Kass S, Tanigawa G, Vosberg H-P, McKenna W, Seidman CE, Seidman J (1990) A molecular basis for familial hypertrophic cardiomyopathy: a β cardiac myosin heavy chain gene missense mutation. Cell 62:999–1006. https://doi.org/10.1016/0092-8674(90)90274-i
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