Mutations in cardiovascular connexin genes
Author:
Affiliation:
1. Department of Pathology and Immunology; Faculty of Medicine; University of Geneva; Geneva Switzerland
2. Department of Medical Specializations - Cardiology; Faculty of Medicine; University of Geneva; Geneva Switzerland
Publisher
Wiley
Subject
Cell Biology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/boc.201400038/fullpdf
Reference188 articles.
1. Evolutionary analyses of gap junction protein families;Abascal;Biochim. Biophys. Acta,2013
2. Gap junctions in inherited human disorders of the central nervous system;Abrams;Biochim. Biophys. Acta,2012
3. Arrhythmogenic cardiomyopathy and Brugada syndrome: diseases of the connexome;Agullo-Pascual;FEBS Lett.,2014
4. Pelizaeus-Merzbacher-like disease in a family with variable phenotype and a novel splicing GJC2 mutation;Al-Yahyaee;J. Child Neurol.,2012
5. Loss of connexin40 is associated with decreased endothelium-dependent relaxations and eNOS levels in the mouse aorta;Alonso;Am. J. Physiol. Heart Circ. Physiol.,2010
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