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A Murine Hypertrophic Cardiomyopathy Model: The DBA/2J Strain
Familial hypertrophic cardiomyopathy (HCM) is attributed to mutations in genes that encode for the sarcomere proteins, especially Mybpc3 and Myh7. Genotype-phenotype correlation studies show significant variability in HCM phenotypes among affected individuals with identical causal mutations. Morphol...
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| Gepubliceerd in: | PLoS One |
|---|---|
| Hoofdauteurs: | , , , , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Public Library of Science
2015
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4524617/ https://ncbi.nlm.nih.gov/pubmed/26241864 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0133132 |
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