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Novel mutations in the sarcomeric protein myopalladin in patients with dilated cardiomyopathy

Recently, missense mutations in titin-associated proteins have been linked to the pathogenesis of dilated cardiomyopathy (DCM). The objective of this study was to search for novel disease-associated mutations in the two human titin-binding proteins myopalladin and its amino-terminal-interacting part...

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Dettagli Bibliografici
Autori principali: Meyer, Thomas, Ruppert, Volker, Ackermann, Sarah, Richter, Anette, Perrot, Andreas, Sperling, Silke R, Posch, Maximilian G, Maisch, Bernhard, Pankuweit, Sabine
Natura: Artigo
Lingua:Inglês
Pubblicazione: Nature Publishing Group 2013
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC3573205/
https://ncbi.nlm.nih.gov/pubmed/22892539
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2012.173
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