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Rapid molecular genetic diagnosis of hypertrophic cardiomyopathy by semiconductor sequencing
BACKGROUND: Rapidly determining the complex genetic basis of Hypertrophic cardiomyopathy (HCM) is vital to better understanding and optimally managing this common polygenetic cardiovascular disease. METHODS: A rapid custom Ion-amplicon-resequencing assay, covering 30 commonly affected genes of HCM,...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4072843/ https://ncbi.nlm.nih.gov/pubmed/24938736 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1479-5876-12-173 |
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