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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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| Hlavní autoři: | , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Blackwell Publishing Inc
2011
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| Témata: | |
| On-line přístup: | 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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