Skip to search boxSkip to navigationSkip to main content

Molecular basis of cardiovascular abnormalities in NF1

*Corresponding author for this work
  • Indiana University Bloomington
    ,
  • University of British Columbia
Scholary Output:
Chapter in Book/Report/Conference proceeding
Chapter

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.

Publication Information

Output type

Scholary Output:
Chapter in Book/Report/Conference proceeding
Chapter

Host publication Subtitle

Molecular and Cellular Biology

Original language

English (US)

Pages from-to (Number of pages)

Pages 353-366 (14 pages)

Publication milestones

  • Published - 08/01/2012

Publication status

Published - 08/01/2012

Volume

9783642328640

Publisher

Springer-Verlag Berlin Heidelberg
3642328636, 9783642328633

ISBN (Electronic)

9783642328640

Publication IDs

  • Scopus: 84949180045

Host publication title

Neurofibromatosis Type 1

Publication metrics

Metrics

SciVal
citations
1
Fractional count
1
Fractional count
0.25
Fractional count
3
Fractional count
0.75
Fractional count
1
Fractional count
1
SciVal
Author count
4
SciVal
Paper percentile
34
Scopus
citations

PlumX, opens in new tab

Captures
6
Citation count
2