Genetics and genotype–phenotype correlations in Finnish patients with dilated cardiomyopathy

AIMS: Despite our increased understanding of the genetic basis of dilated cardiomyopathy (DCM), the clinical utility and yield of clinically meaningful findings of comprehensive next-generation sequencing (NGS)-based genetic diagnostics in DCM has been poorly described. We utilized a high-quality ol...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Eur Heart J
Prif Awduron: Akinrinade, Oyediran, Ollila, Laura, Vattulainen, Sanna, Tallila, Jonna, Gentile, Massimiliano, Salmenperä, Pertteli, Koillinen, Hannele, Kaartinen, Maija, Nieminen, Markku S., Myllykangas, Samuel, Alastalo, Tero-Pekka, Koskenvuo, Juha W., Heliö, Tiina
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Oxford University Press 2015
Pynciau:
Basic Science
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC4561350/
https://ncbi.nlm.nih.gov/pubmed/26084686
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/eurheartj/ehv253
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