Obscurin variants and inherited cardiomyopathies
Author:
Funder
British Heart Foundation
Publisher
Springer Science and Business Media LLC
Subject
Molecular Biology,Structural Biology,Biophysics
Link
http://link.springer.com/article/10.1007/s12551-017-0264-8/fulltext.html
Reference28 articles.
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2. Ackermann MA, Shriver M, Perry NA, Hu L-YR, Kontrogianni-Konstantopoulos A (2014) Obscurins: goliaths and Davids take over non-muscle tissues. PLoS ONE 9:e88162. doi: 10.1371/journal.pone.0088162.s003
3. Alfares AA et al (2015) Results of clinical genetic testing of 2,912 probands with hypertrophic cardiomyopathy: expanded panels offer limited additional sensitivity. Genet Med 17:880–888. doi: 10.1038/gim.2014.205
4. Arimura T et al (2007) Structural analysis of obscurin gene in hypertrophic cardiomyopathy. Biochem Biophys Res Commun 362:281–287. doi: 10.1016/j.bbrc.2007.07.183
5. Bagnato P, Barone V, Giacomello E, Rossi D, Sorrentino V (2003) Binding of an ankyrin-1 isoform to obscurin suggests a molecular link between the sarcoplasmic reticulum and myofibrils in striated muscles. J Cell Biol 160:245–253. doi: 10.1083/jcb.200208109
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