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Exome sequencing identifies a mutation in the ACTN2 gene in a family with idiopathic ventricular fibrillation, left ventricular noncompaction, and sudden death

Crossref DOI link: https://doi.org/10.1186/s12881-014-0099-0

Published Online: 2014-09-16

Published Print: 2014-12

Update policy: https://doi.org/10.1007/springer_crossmark_policy

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