Your browser doesn't support javascript.
loading
The clinical outcome of LMNA missense mutations can be associated with the amount of mutated protein in the nuclear envelope.
Al-Saaidi, Rasha A; Rasmussen, Torsten B; Birkler, Rune I D; Palmfeldt, Johan; Beqqali, Abdelaziz; Pinto, Yigal M; Nissen, Peter H; Baandrup, Ulrik; Mølgaard, Henning; Hey, Thomas M; Eiskjaer, Hans; Bross, Peter; Mogensen, Jens.
Afiliación
  • Al-Saaidi RA; Research Unit for Molecular Medicine, Aarhus University and University Hospital, Aarhus, Denmark.
  • Rasmussen TB; Department of Cardiology, Aarhus University Hospital, Aarhus, Denmark.
  • Birkler RID; Research Unit for Molecular Medicine, Aarhus University and University Hospital, Aarhus, Denmark.
  • Palmfeldt J; Research Unit for Molecular Medicine, Aarhus University and University Hospital, Aarhus, Denmark.
  • Beqqali A; Centre for Cardiovascular Science, University of Edinburgh, Edinburgh, UK.
  • Pinto YM; Heart Failure Research Center, Academic Medical Center, Amsterdam, The Netherlands.
  • Nissen PH; Department of Clinical Biochemistry, Aarhus University Hospital, Aarhus, Denmark.
  • Baandrup U; Centre for Clinical Research, North Denmark Regional Hospital/Department of Clinical Medicine, Aalborg University, Aalborg, Denmark.
  • Mølgaard H; Department of Cardiology, Aarhus University Hospital, Aarhus, Denmark.
  • Hey TM; Department of Cardiology, Odense University Hospital, Odense, Denmark.
  • Eiskjaer H; Department of Cardiology, Aarhus University Hospital, Aarhus, Denmark.
  • Bross P; Research Unit for Molecular Medicine, Aarhus University and University Hospital, Aarhus, Denmark.
  • Mogensen J; Department of Cardiology, Odense University Hospital, Odense, Denmark.
Eur J Heart Fail ; 20(10): 1404-1412, 2018 10.
Article en En | MEDLINE | ID: mdl-29943882
Asunto(s)
Palabras clave
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: ADN / Predisposición Genética a la Enfermedad / Mutación Missense / Lamina Tipo A / Insuficiencia Cardíaca / Miocardio Tipo de estudio: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Eur J Heart Fail Asunto de la revista: CARDIOLOGIA Año: 2018 Tipo del documento: Article País de afiliación: Dinamarca
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: ADN / Predisposición Genética a la Enfermedad / Mutación Missense / Lamina Tipo A / Insuficiencia Cardíaca / Miocardio Tipo de estudio: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Eur J Heart Fail Asunto de la revista: CARDIOLOGIA Año: 2018 Tipo del documento: Article País de afiliación: Dinamarca