Inherited Extremes of Aortic Diameter Confer Risk for a Specific Class of Congenital Heart Disease

Circ Genom Precis Med. 2020 Dec;13(6):e003170. doi: 10.1161/CIRCGEN.120.003170. Epub 2020 Nov 15.

Authors

Catherine Tcheandjieu^{1

2

3}, Daniela Zanetti^{2

3}, Mengyao Yu^{1

3}, James R Priest^{1

3

4}

Affiliations

¹ Division of Pediatric Cardiology, Department of Pediatrics (C.T., M.Y., J.R.P.), Stanford University School of Medicine, CA.
² Division of Cardiovascular Medicine, Department of Medicine (C.T., D.Z.), Stanford University School of Medicine, CA.
³ Stanford Cardiovascular Institute, Stanford University, CA (C.T., D.Z., M.Y., J.R.P.).
⁴ Chan-Zuckerberg Biohub, San Francisco, CA (J.R.P.).

PMID: 33191768
DOI: 10.1161/CIRCGEN.120.003170

No abstract available

Keywords: aorta; embryology; heart diseases; mutation; risk factors.

Publication types

Letter
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't

MeSH terms

Aorta / pathology*
Heart Defects, Congenital / classification*
Heart Defects, Congenital / diagnostic imaging
Heart Defects, Congenital / genetics*
Humans
Inheritance Patterns / genetics*
Magnetic Resonance Imaging
Risk Factors

Grants and funding

R00 HL130523/HL/NHLBI NIH HHS/United States