Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilate...
Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy
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Publisher
New York, NY: Mosby, Inc
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Language
English
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Publisher
New York, NY: Mosby, Inc
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Contents
Background Lamin A/C mutations are a well-established cause of dilated cardiomyopathy (DCM), although their frequency has not been examined in a large cohort of patients. We sought to examine the frequency of mutations in LMNA , the gene encoding lamin A/C, in patients with idiopathic (IDC) or familial dilated cardiomyopathy (FDC). Methods Clinical...
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Full title
Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy
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TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2527054
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2527054
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ISSN
0002-8703
E-ISSN
1097-6744
DOI
10.1016/j.ahj.2008.01.026
