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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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Autori principali: Norton, Nadine, Siegfried, Jill D., Li, Duanxiang, Hershberger, Ray E.
Natura: Artigo
Lingua:Inglês
Pubblicazione: Blackwell Publishing Inc 2011
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Accesso online: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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