Identification of MYLK3 mutations in familial dilated cardiomyopathy-Reference-Cited by-同舟云学术

Identification of MYLK3 mutations in familial dilated cardiomyopathy

Published:2017-12 Issue:1 Volume:7 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Tobita Takashige,Nomura Seitaro,Morita Hiroyuki,Ko Toshiyuki,Fujita Takanori,Toko Haruhiro,Uto Kenta,Hagiwara Nobuhisa,Aburatani Hiroyuki^ORCID,Komuro Issei

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/s41598-017-17769-1.pdf

Reference36 articles.

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3. Boycott, K. M., Vanstone, M. R., Bulman, D. E. & MacKenzie, A. E. Rare-disease genetics in the era of next-generation sequencing: discovery to translation. Nat. Rev. Genet. 14, 681–691 (2013).

4. Seguchi, O. et al. A cardiac myosin light chain kinase regulates sarcomere assembly in the vertebrate heart. J Clin Invest. 117, 2812–2824 (2007).

5. Chan, J. Y. et al. Identification of cardiac-specific myosin light chain kinase. Circ Res. 102, 571–580 (2008).

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