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Genetic Screening Reveals Heterogeneous Clinical Phenotypes in Patients with Dilated Cardiomyopathy and Troponin T2 Variants.
Weis, Angelika; Krueck, Svenja; Dombrowsky, Gregor; Schänzer, Anne; Jux, Christian; Uebing, Anselm; Voges, Inga; Hitz, Marc-Phillip; Rupp, Stefan.
Afiliação
  • Weis A; Department of Pediatric Cardiology, Intensive Care Medicine and Congenital Heart Disease, Justus Liebig University Giessen, 35390 Giessen, Germany.
  • Krueck S; Department of Pediatric Cardiology, Intensive Care Medicine and Congenital Heart Disease, Justus Liebig University Giessen, 35390 Giessen, Germany.
  • Dombrowsky G; Department of Congenital Heart Disease and Pediatric Cardiology, University Hospital of Schleswig-Holstein, 24105 Kiel, Germany.
  • Schänzer A; Institute of Medical Genetics, Carl von Ossietzky University, 26129 Oldenburg, Germany.
  • Jux C; Institute of Neuropathology, Justus Liebig University Giessen, 35390 Giessen, Germany.
  • Uebing A; Department of Pediatric Cardiology, Intensive Care Medicine and Congenital Heart Disease, Justus Liebig University Giessen, 35390 Giessen, Germany.
  • Voges I; Department of Congenital Heart Disease and Pediatric Cardiology, University Hospital of Schleswig-Holstein, 24105 Kiel, Germany.
  • Hitz MP; DZHK (German Centre for Cardiovascular Research), Partner Site Hamburg/Lübeck/Kiel, 24105 Kiel, Germany.
  • Rupp S; Department of Congenital Heart Disease and Pediatric Cardiology, University Hospital of Schleswig-Holstein, 24105 Kiel, Germany.
J Pers Med ; 13(4)2023 Mar 31.
Article em En | MEDLINE | ID: mdl-37108997

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article