TNNI3K mutation in familial syndrome of conduction system disease, atrial tachyarrhythmia and dilated cardiomyopathy

Locus mapping has uncovered diverse etiologies for familial atrial fibrillation (AF), dilated cardiomyopathy (DCM), and mixed cardiac phenotype syndromes, yet the molecular basis for these disorders remains idiopathic in most cases. Whole-exome sequencing (WES) provides a powerful new tool for famil...

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Autors principals: Theis, Jeanne L., Zimmermann, Michael T., Larsen, Brandon T., Rybakova, Inna N., Long, Pamela A., Evans, Jared M., Middha, Sumit, de Andrade, Mariza, Moss, Richard L., Wieben, Eric D., Michels, Virginia V., Olson, Timothy M.
Format: Artigo
Idioma:Inglês
Publicat: Oxford University Press 2014
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Articles
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4189907/
https://ncbi.nlm.nih.gov/pubmed/24925317
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddu297
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