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Expanding the phenotype of sudden cardiac death: an unusual presentation of a family with a Lamin A/C mutation

Julie De Backer (UGent) , KATARINA VAN BEEUMEN (UGent) , Bart Loeys (UGent) and Mattias Duytschaever (UGent)
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Organization
Abstract
Familial occurrence of sudden cardiac death (SCD) is related to a variety of clinical conditions, which can be delineated in up to 40% of families through a combination of cardiovascular examination and genetic studies. Patients with Lamin A/C gene mutations are at increased risk for SCD, but "laminopathies" are not included into clinical algorithms of SCD.
Keywords
AV conduction disease, CONDUCTION-SYSTEM, Lamin A/C, Sudden cardiac death, GENE-MUTATIONS, DISEASE

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Citation

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MLA
De Backer, Julie et al. “Expanding the Phenotype of Sudden Cardiac Death: An Unusual Presentation of a Family with a Lamin A/C Mutation.” INTERNATIONAL JOURNAL OF CARDIOLOGY 138.1 (2010): 97–99. Print.
APA
De Backer, J., VAN BEEUMEN, K., Loeys, B., & Duytschaever, M. (2010). Expanding the phenotype of sudden cardiac death: an unusual presentation of a family with a Lamin A/C mutation. INTERNATIONAL JOURNAL OF CARDIOLOGY, 138(1), 97–99.
Chicago author-date
De Backer, Julie, KATARINA VAN BEEUMEN, Bart Loeys, and Mattias Duytschaever. 2010. “Expanding the Phenotype of Sudden Cardiac Death: An Unusual Presentation of a Family with a Lamin A/C Mutation.” International Journal of Cardiology 138 (1): 97–99.
Chicago author-date (all authors)
De Backer, Julie, KATARINA VAN BEEUMEN, Bart Loeys, and Mattias Duytschaever. 2010. “Expanding the Phenotype of Sudden Cardiac Death: An Unusual Presentation of a Family with a Lamin A/C Mutation.” International Journal of Cardiology 138 (1): 97–99.
Vancouver
1.
De Backer J, VAN BEEUMEN K, Loeys B, Duytschaever M. Expanding the phenotype of sudden cardiac death: an unusual presentation of a family with a Lamin A/C mutation. INTERNATIONAL JOURNAL OF CARDIOLOGY. 2010;138(1):97–9.
IEEE
[1]
J. De Backer, K. VAN BEEUMEN, B. Loeys, and M. Duytschaever, “Expanding the phenotype of sudden cardiac death: an unusual presentation of a family with a Lamin A/C mutation,” INTERNATIONAL JOURNAL OF CARDIOLOGY, vol. 138, no. 1, pp. 97–99, 2010.
@article{889436,
  abstract     = {Familial occurrence of sudden cardiac death (SCD) is related to a variety of clinical conditions, which can be delineated in up to 40% of families through a combination of cardiovascular examination and genetic studies. Patients with Lamin A/C gene mutations are at increased risk for SCD, but "laminopathies" are not included into clinical algorithms of SCD.},
  author       = {De Backer, Julie and VAN BEEUMEN, KATARINA and Loeys, Bart and Duytschaever, Mattias},
  issn         = {0167-5273},
  journal      = {INTERNATIONAL JOURNAL OF CARDIOLOGY},
  keywords     = {AV conduction disease,CONDUCTION-SYSTEM,Lamin A/C,Sudden cardiac death,GENE-MUTATIONS,DISEASE},
  language     = {eng},
  number       = {1},
  pages        = {97--99},
  title        = {Expanding the phenotype of sudden cardiac death: an unusual presentation of a family with a Lamin A/C mutation},
  url          = {http://dx.doi.org/10.1016/j.ijcard.2008.06.008},
  volume       = {138},
  year         = {2010},
}

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