Absence of TGFBR1 and TGFBR2 Mutations in Patients With Bicuspid Aortic Valve and Aortic Dilation
Author:
Publisher
Elsevier BV
Subject
Cardiology and Cardiovascular Medicine
Reference12 articles.
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2. Mutations in NOTCH1 cause aortic valve disease;Garg;Nature,2005
3. Novel NOTCH1 mutations in patients with bicuspid aortic valve disease and thoracic aortic aneurysms;McKellar;J Thorac Cardiovasc Surg,2007
4. A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2;Loeys;Nat Genet,2005
5. Familial thoracic aortic dilation and bicommissural aortic valve: a prospective analysis of natural history and inheritance;Loscalzo;Am J Med Genet A,2007
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1. CRELD1 variants are associated with bicuspid aortic valve in Turner syndrome;Human Genetics;2023-03-16
2. Bicuspidalization of the Native Tricuspid Aortic Valve: A Porcine in Vivo Model of Bicuspid Aortopathy;Annals of Vascular Diseases;2022-03-25
3. Aortic Dilatation in Patients With Bicuspid Aortic Valve;Frontiers in Physiology;2021-07-06
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5. Genetics in bicuspid aortic valve disease: Where are we?;Progress in Cardiovascular Diseases;2020-07
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