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Most read last month
  • Targeted capture and massively parallel sequencing in pediatric cardiomyopathy: development of novel diagnostics
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  • Combined use of in silico and in vitro splicing assays for interpretation of genomic variants of unknown significance in cardiomyopathies and channelopathies
    73
  • Novel SCN5A mutation associated with idiopathic ventricular fibrillation due to subclinical Brugada syndrome
    68
  • LQTS-associated mutation A257G in α1-syntrophin interacts with the intragenic variant P74L to modify its biophysical phenotype
    67
  • Cardiac electrical system involvement in Alström syndrome: uncommon causes of dilated cardiomyopathies
    62
Keywords
Cardiogenetics

is an Open Access, peer-reviewed journal published by PAGEPress®, Pavia, Italy. All credits and honors to PKP for their OJS.

eISSN 2035-8148

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