Molecular basis of cardiovascular abnormalities in NF1

Brian K. Stansfield, David A. Ingram, Simon J. Conway, Jan M. Friedman

Research output: Chapter in Book/Report/Conference proceedingChapter

1 Scopus citations

Abstract

Congenital heart defects are uncommon among people with NF1, but pulmonic stenosis and coarctation of the aorta appear to occur more often than expected. Double outlet right ventricle (the characteristic cardiac defect in Nf1 -/- mouse models) and other complex cardiac malformations are rare in people with NF1.

Original languageEnglish (US)
Title of host publicationNeurofibromatosis Type 1
Subtitle of host publicationMolecular and Cellular Biology
PublisherSpringer-Verlag Berlin Heidelberg
Pages353-366
Number of pages14
Volume9783642328640
ISBN (Electronic)9783642328640
ISBN (Print)3642328636, 9783642328633
DOIs
StatePublished - Aug 1 2012
Externally publishedYes

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ASJC Scopus subject areas

  • Medicine(all)
  • Biochemistry, Genetics and Molecular Biology(all)

Cite this

Stansfield, B. K., Ingram, D. A., Conway, S. J., & Friedman, J. M. (2012). Molecular basis of cardiovascular abnormalities in NF1. In Neurofibromatosis Type 1: Molecular and Cellular Biology (Vol. 9783642328640, pp. 353-366). Springer-Verlag Berlin Heidelberg. https://doi.org/10.1007/978-3-642-32864-0_23