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

Overview

Published in

  • BMC Medical Genetics

Time

Date/time value

  • 2014

Identity

Digital Object Identifier (DOI)

  • 10.1186/s12881-014-0099

Additional Document Info

Parent Title

  • BMC MEDICAL GENETICS

Volume

  • 15

Number

  • ARTN 99

Publisher

  • Biomed Central