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Morphological analysis of 13 LMNA variants identified in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy
BACKGROUND: Mutations in the LMNA gene, encoding lamins A/C, represent a significant cause of dilated cardiomyopathy (DCM). We recently identified 18 protein-altering LMNA variants in a cohort of 324 unrelated patients with DCM. However, at least one family member with DCM in each of six pedigrees l...
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| Hoofdauteurs: | , , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
2009
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2908895/ https://ncbi.nlm.nih.gov/pubmed/20160190 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/CIRCGENETICS.109.905422 |
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