Abnormal spirometry in adults with 22q11.2 microdeletion and congenital heart disease
Background: In adults with congenital heart disease (CHD), pulmonary dysfunction is prevalent and associated with poor outcomes; however, underlying genetic contributors remain unexamined. We investigated whether the 22q11.2 microdeletion, an important genetic cause of CHD, was associated with abnor...
Main Authors: | , , , , , , |
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Format: | Article |
Language: | English |
Published: |
Elsevier
2021-05-01
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Series: | International Journal of Cardiology Congenital Heart Disease |
Subjects: | |
Online Access: | http://www.sciencedirect.com/science/article/pii/S2666668521000094 |