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Multinational experience with next-generation sequencing: opportunity to identify transthyretin cardiac amyloidosis and Fabry disease.

Sandra Marques E SilvaAndrea Virginia Ferreira ChavesMurillo AntunesJuan Pablo CostabelArmando Alves da FonsecaAdriana FurtadoJuan Esteban Gomez-MesaFrancisco Javier Marin GutiérrezOren CaspiIrina MaksimovaManish MaskiCecilia MichelettiJosé Luiz Barros PenaMárcia Gonçalves RibeiroMaria Juliana Rodríguez-GonzálezOmac TufekciogluHüseyin Onay
Published in: Cardiovascular diagnosis and therapy (2024)
variants), which are treatable disorders, in the differential diagnosis of patients with increased LVWT of unknown etiology.
Keyphrases
  • copy number
  • left ventricular
  • replacement therapy
  • hypertrophic cardiomyopathy
  • multiple myeloma
  • genome wide
  • wild type
  • gene expression