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,...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Zongzhe, Huang, Jin, Zhao, Jinzhao, Chen, Chen, Wang, Hong, Ding, Hu, Wang, Dao Wu, Wang, Dao Wen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Methodology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4072843/
https://www.ncbi.nlm.nih.gov/pubmed/24938736
http://dx.doi.org/10.1186/1479-5876-12-173

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4072843/
https://www.ncbi.nlm.nih.gov/pubmed/24938736
http://dx.doi.org/10.1186/1479-5876-12-173

Ejemplares similares