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Rare genomic copy number variants implicate new candidate genes for bicuspid aortic valve

Rare genomic copy number variants implicate new candidate genes for bicuspid aortic valve

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_3101517196

Rare genomic copy number variants implicate new candidate genes for bicuspid aortic valve

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Publication information

Publisher

United States: Public Library of Science

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Scope and Contents

Contents

Bicuspid aortic valve (BAV), the most common congenital heart defect, is a major cause of aortic valve disease requiring valve interventions and thoracic aortic aneurysms predisposing to acute aortic dissections. The spectrum of BAV ranges from early onset valve and aortic complications (EBAV) to sporadic late onset disease. Rare genomic copy numbe...

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Full title

Rare genomic copy number variants implicate new candidate genes for bicuspid aortic valve

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Primary Identifiers

Record Identifier

TN_cdi_plos_journals_3101517196

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_3101517196

Other Identifiers

ISSN

1932-6203

E-ISSN

1932-6203

DOI

10.1371/journal.pone.0304514

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