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Genetic Insights from Consanguineous Cardiomyopathy Families.
Maurer, Constance; Boleti, Olga; Najarzadeh Torbati, Paria; Norouzi, Farzaneh; Fowler, Anna Nicole Rebekah; Minaee, Shima; Salih, Khalid Hama; Taherpour, Mehdi; Birjandi, Hassan; Alizadeh, Behzad; Salih, Aso Faeq; Bijari, Moniba; Houlden, Henry; Pittman, Alan Michael; Maroofian, Reza; Almashham, Yahya H; Karimiani, Ehsan Ghayoor; Kaski, Juan Pablo; Faqeih, Eissa Ali; Vakilian, Farveh; Jamshidi, Yalda.
Afiliação
  • Maurer C; Genetics Research Centre, Molecular and Clinical Sciences Institute, St George's, University of London, Cranmer Terrace, London SW17 0RE, UK.
  • Boleti O; Centre for Paediatric Inherited and Rare Cardiovascular Disease, University College London and Great Ormond Street Hospital, London WC1N 1DZ, UK.
  • Najarzadeh Torbati P; Department of Medical Genetics, Next Generation Genetic Polyclinic, Mashhad 009851, Iran.
  • Norouzi F; Department of Cardiology, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad 9177948564, Iran.
  • Fowler ANR; Genetics Research Centre, Molecular and Clinical Sciences Institute, St George's, University of London, Cranmer Terrace, London SW17 0RE, UK.
  • Minaee S; Department of Cardiovascular Diseases, Razavi Hospital, Mashhad 9177948954, Iran.
  • Salih KH; Department of Pediatrics, College of Medicine, Sulaimani University, Sulaymaniyah 46001, Iraq.
  • Taherpour M; Department of Cardiovascular Diseases, Razavi Hospital, Mashhad 9177948954, Iran.
  • Birjandi H; Division of Congenital and Pediatric Cardiology, Department of Pediatrics, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad 9177948564, Iran.
  • Alizadeh B; Division of Congenital and Pediatric Cardiology, Department of Pediatrics, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad 9177948564, Iran.
  • Salih AF; Department of Pediatrics, College of Medicine, Sulaimani University, Sulaymaniyah 46001, Iraq.
  • Bijari M; Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad 9177948564, Iran.
  • Houlden H; Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, University College London, London WC1N 3BG, UK.
  • Pittman AM; Genetics Research Centre, Molecular and Clinical Sciences Institute, St George's, University of London, Cranmer Terrace, London SW17 0RE, UK.
  • Maroofian R; Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, University College London, London WC1N 3BG, UK.
  • Almashham YH; Pediatric Cardiology, King Salman Heart Center, King Fahad Medical City, Riyadh 12231, Saudi Arabia.
  • Karimiani EG; Genetics Research Centre, Molecular and Clinical Sciences Institute, St George's, University of London, Cranmer Terrace, London SW17 0RE, UK.
  • Kaski JP; Department of Medical Genetics, Next Generation Genetic Polyclinic, Mashhad 009851, Iran.
  • Faqeih EA; Centre for Paediatric Inherited and Rare Cardiovascular Disease, University College London and Great Ormond Street Hospital, London WC1N 1DZ, UK.
  • Vakilian F; Section of Medical Genetics, Children's Specialist Hospital, King Fahad Medical City, Riyadh 12231, Saudi Arabia.
  • Jamshidi Y; Department of Cardiology, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad 9177948564, Iran.
Genes (Basel) ; 14(1)2023 01 10.
Article em En | MEDLINE | ID: mdl-36672924
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cardiomiopatia Dilatada / Cardiomiopatias Tipo de estudo: Prognostic_studies Limite: Child, preschool / Humans Idioma: En Revista: Genes (Basel) Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Reino Unido
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cardiomiopatia Dilatada / Cardiomiopatias Tipo de estudo: Prognostic_studies Limite: Child, preschool / Humans Idioma: En Revista: Genes (Basel) Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Reino Unido