The K219T-Lamin mutation induces conduction defects through epigenetic inhibition of SCN5A in human cardiac laminopathy
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry
Link
http://www.nature.com/articles/s41467-019-09929-w.pdf
Reference71 articles.
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2. Dechat, T. et al. Nuclear lamins: major factors in the structural organization and function of the nucleus and chromatin. Genes Dev. 22, 832–853 (2008).
3. Hershberger, R. E., Hedges, D. J. & Morales, A. Dilated cardiomyopathy: the complexity of a diverse genetic architecture. Nat. Rev. Cardiol. 10, 531–547 (2013).
4. Rankin, J. & Ellard, S. The laminopathies: a clinical review. Clin. Genet. 70, 261–274 (2006).
5. Worman, H. J. & Bonne, G. “Laminopathies”: a wide spectrum of human diseases. Exp. Cell Res. 313, 2121–2133 (2007).
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