Συγγραφείς:
Sanoudou, D.
Kolokathis, F.
Arvanitis, D.
Al-Shafai, K.
Krishnamoorthy, N.
Buchan, R.J.
Walsh, R.
Tsiapras, D.
Barton, P.J.R.
Cook, S.A.
Kremastinos, D.
Yacoub, M.
Λέξεις-κλειδιά:
merosin, adult; Alstrom Syndrome 1 gene; Article; atrial fibrillation; CACNB2 gene; case report; congestive cardiomyopathy; death; frameshift mutation; genotype phenotype correlation; heart left ventricle ejection fraction; heart left ventricle hypertrophy; heart ventricle extrasystole; heart ventricle tachycardia; heterozygote; high throughput sequencing; hospital readmission; human; implantable cardioverter defibrillator; laminin 2 gene; left ventricular systolic dysfunction; male; middle aged; modifier gene; next generation sequencing; nonsense mutation; PLN gene; single nucleotide polymorphism; sustained ventricular tachycardia
