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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.

• Authors : Bagnall RD; Agnes Ginges Centre for Molecular Cardiology, Centenary Institute, Locked Bag 6, Newtown, Sydney, NSW, 2042, Australia. .; Faculty of Medicine, University of Sydney, Sydney, NSW, Australia. .

Subjects: Actinin/Actinin/Actinin/*genetics ; Death, Sudden, Cardiac/Death, Sudden, Cardiac/Death, Sudden, Cardiac/*etiology ; Heart Defects, Congenital/Heart Defects, Congenital/Heart Defects, Congenital/*genetics Noncompaction of Left Ventricular Myocardium with Congenital Heart Defects

• Source: BMC medical genetics [BMC Med Genet] 2014 Sep 16; Vol. 15, pp. 99. Date of Electronic Publication: 2014 Sep 16.Publisher: BioMed Central Country of Publication: England NLM ID: 100968552 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2350

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