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Research priorities in sarcomeric cardiomyopathies

The clinical variability in patients with sarcomeric cardiomyopathies is striking: a mutation causes cardiomyopathy in one individual, while the identical mutation is harmless in a family member. Moreover, the clinical phenotype varies ranging from asymmetric hypertrophy to severe dilatation of the...

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Publicado en:Cardiovasc Res
Autores principales: van der Velden, Jolanda, Ho, Carolyn Y., Tardiff, Jil C., Olivotto, Iacopo, Knollmann, Bjorn C., Carrier, Lucie
Formato: Artigo
Lenguaje:Inglês
Publicado: Oxford University Press 2015
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC4375392/
https://ncbi.nlm.nih.gov/pubmed/25631582
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/cvr/cvv019
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