Molecular basis of cardiovascular abnormalities in NF1

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

doi:10.1007/978-3-642-32864-0_23

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 proceeding › Chapter

2 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 language	English (US)
Title of host publication	Neurofibromatosis Type 1
Subtitle of host publication	Molecular and Cellular Biology
Publisher	Springer-Verlag Berlin Heidelberg
Pages	353-366
Number of pages	14
Volume	9783642328640
ISBN (Electronic)	9783642328640
ISBN (Print)	3642328636, 9783642328633
DOIs	https://doi.org/10.1007/978-3-642-32864-0_23
State	Published - Aug 1 2012
Externally published	Yes

ASJC Scopus subject areas

General Medicine
General Biochemistry, Genetics and Molecular Biology

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10.1007/978-3-642-32864-0_23

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AB - 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.

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Molecular basis of cardiovascular abnormalities in NF1

Abstract

ASJC Scopus subject areas

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