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A mutation update for the FLNC gene in myopathies and cardiomyopathies.
Verdonschot, Job A J; Vanhoutte, Els K; Claes, Godelieve R F; Helderman-van den Enden, Apollonia T J M; Hoeijmakers, Janneke G J; Hellebrekers, Debby M E I; de Haan, Amber; Christiaans, Imke; Lekanne Deprez, Ronald H; Boen, Hanne M; van Craenenbroeck, Emeline M; Loeys, Bart L; Hoedemaekers, Yvonne M; Marcelis, Carlo; Kempers, Marlies; Brusse, Esther; van Waning, Jaap I; Baas, Annette F; Dooijes, Dennis; Asselbergs, Folkert W; Barge-Schaapveld, Daniela Q C M; Koopman, Pieter; van den Wijngaard, Arthur; Heymans, Stephane R B; Krapels, Ingrid P C; Brunner, Han G.
Afiliación
  • Verdonschot JAJ; Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, The Netherlands.
  • Vanhoutte EK; Department of Cardiology, Cardiovascular Research Institute (CARIM), Maastricht University Medical Center, Maastricht, The Netherlands.
  • Claes GRF; Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, The Netherlands.
  • Helderman-van den Enden ATJM; Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, The Netherlands.
  • Hoeijmakers JGJ; Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, The Netherlands.
  • Hellebrekers DMEI; Department of Neurology, Maastricht University Medical Center, Maastricht, The Netherlands.
  • de Haan A; Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, The Netherlands.
  • Christiaans I; Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, The Netherlands.
  • Lekanne Deprez RH; Department of Clinical Genetics, Amsterdam University Medical Center, Amsterdam, The Netherlands.
  • Boen HM; Department of Clinical Genetics, University Medical Centre Groningen, Groningen, The Netherlands.
  • van Craenenbroeck EM; Department of Clinical Genetics, Amsterdam University Medical Center, Amsterdam, The Netherlands.
  • Loeys BL; Department of Cardiology, Antwerp University Hospital, University of Antwerp, Antwerp, Belgium.
  • Hoedemaekers YM; Department of Cardiology, Antwerp University Hospital, University of Antwerp, Antwerp, Belgium.
  • Marcelis C; Department of Medical Genetics, Antwerp University Hospital, University of Antwerp, Antwerp, Belgium.
  • Kempers M; Department of Clinical Genetics, University Medical Centre Groningen, Groningen, The Netherlands.
  • Brusse E; Department of Clinical Genetics, Radboud University Medical Centre, Nijmegen, The Netherlands.
  • van Waning JI; Department of Clinical Genetics, Radboud University Medical Centre, Nijmegen, The Netherlands.
  • Baas AF; Department of Clinical Genetics, Radboud University Medical Centre, Nijmegen, The Netherlands.
  • Dooijes D; Department of Neurology, Erasmus MC University Medical Centre, Rotterdam, The Netherlands.
  • Asselbergs FW; Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands.
  • Barge-Schaapveld DQCM; Department of Cardiology, Radboud University Medical Centre, Nijmegen, The Netherlands.
  • Koopman P; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
  • van den Wijngaard A; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Heymans SRB; Department of Cardiology, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Krapels IPC; Department of Clinical Genetics, Leiden University Medical Center, The Netherlands.
  • Brunner HG; Department of Cardiology, Heart Center Hasselt, Belgium.
Hum Mutat ; 41(6): 1091-1111, 2020 06.
Article en En | MEDLINE | ID: mdl-32112656
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Filaminas / Enfermedades Musculares / Cardiomiopatías Límite: Animals / Humans Idioma: En Revista: Hum Mutat Asunto de la revista: GENETICA MEDICA Año: 2020 Tipo del documento: Article País de afiliación: Países Bajos
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Filaminas / Enfermedades Musculares / Cardiomiopatías Límite: Animals / Humans Idioma: En Revista: Hum Mutat Asunto de la revista: GENETICA MEDICA Año: 2020 Tipo del documento: Article País de afiliación: Países Bajos