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Lamin A/C Missense Mutation R216C Pinpoints Overlapping Features Between Brugada Syndrome and Laminopathies.
Armaroli, Annarita; Balla, Cristina; Trabanelli, Cecilia; Selvatici, Rita; Brieda, Alessandro; Sette, Elisabetta; Bertini, Matteo; Mele, Donato; Biffi, Mauro; Campo, Gianluca Calogero; Ferrari, Roberto; Ferlini, Alessandra; Gualandi, Francesca.
Affiliation
  • Armaroli A; Medical Genetics Unit (A.A., C.T., R.S., A.F., F.G.), S. Anna University Hospital, Ferrara.
  • Balla C; Cardiology Unit (C.B., A.B., M. Bertini, D.M., G.C.C., R.F.), S. Anna University Hospital, Ferrara.
  • Trabanelli C; Medical Genetics Unit (A.A., C.T., R.S., A.F., F.G.), S. Anna University Hospital, Ferrara.
  • Selvatici R; Medical Genetics Unit (A.A., C.T., R.S., A.F., F.G.), S. Anna University Hospital, Ferrara.
  • Brieda A; Cardiology Unit (C.B., A.B., M. Bertini, D.M., G.C.C., R.F.), S. Anna University Hospital, Ferrara.
  • Sette E; Neurology Unit (E.S.), S. Anna University Hospital, Ferrara.
  • Bertini M; Cardiology Unit (C.B., A.B., M. Bertini, D.M., G.C.C., R.F.), S. Anna University Hospital, Ferrara.
  • Mele D; Cardiology Unit (C.B., A.B., M. Bertini, D.M., G.C.C., R.F.), S. Anna University Hospital, Ferrara.
  • Biffi M; Department of Experimental, Diagnostic and Specialty Medicine, University of Bologna, S. Orsola-Malpighi University Hospital (M. Biffi\).
  • Campo GC; Cardiology Unit (C.B., A.B., M. Bertini, D.M., G.C.C., R.F.), S. Anna University Hospital, Ferrara.
  • Ferrari R; Maria Cecilia Hospital, GVM Care & Research, Cotignola, Italy (G.C.C., R.F.).
  • Ferlini A; Cardiology Unit (C.B., A.B., M. Bertini, D.M., G.C.C., R.F.), S. Anna University Hospital, Ferrara.
  • Gualandi F; Maria Cecilia Hospital, GVM Care & Research, Cotignola, Italy (G.C.C., R.F.).
Circ Genom Precis Med ; 13(2): e002751, 2020 04.
Article in En | MEDLINE | ID: mdl-32155092
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Full text: 1 Database: MEDLINE Main subject: Mutation, Missense / Lamin Type A / Brugada Syndrome / Laminopathies Type of study: Prognostic_studies Limits: Adult / Humans / Male Language: En Journal: Circ Genom Precis Med Year: 2020 Type: Article
Fulltext
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Full text: 1 Database: MEDLINE Main subject: Mutation, Missense / Lamin Type A / Brugada Syndrome / Laminopathies Type of study: Prognostic_studies Limits: Adult / Humans / Male Language: En Journal: Circ Genom Precis Med Year: 2020 Type: Article