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Assessment of LMNA Copy Number Variation in 58 Probands with Dilated Cardiomyopathy

The contribution of copy number variation (CNV) to dilated cardiomyopathy (DCM) is unknown. However, estimates have suggested that CNVs could constitute 15% of mutations underlying Mendelian disease. This is of particular relevance to DCM, where only approximately 35% of genetic cause has been ident...

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Detalhes bibliográficos
Main Authors: Norton, Nadine, Siegfried, Jill D., Li, Duanxiang, Hershberger, Ray E.
Formato: Artigo
Idioma:Inglês
Publicado em: Blackwell Publishing Inc 2011
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3205425/
https://ncbi.nlm.nih.gov/pubmed/22029807
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1752-8062.2011.00305.x
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