APA (7th ed.) Citation

Chesneau, B., Plancke, A., Rolland, G., Marcheix, B., Dulac, Y., Edouard, T., . . . Kien, P. K. V. (2021). A +3 variant at a donor splice site leads to a skipping of the MYH11 exon 32, a recurrent RNA defect causing Heritable Thoracic Aortic Aneurysm and Dissection and/or Patent Ductus Arteriosus. Wiley.

Chicago Style (17th ed.) Citation

Chesneau, Bertrand, et al. A +3 Variant at a Donor Splice Site Leads to a Skipping of the MYH11 Exon 32, a Recurrent RNA Defect Causing Heritable Thoracic Aortic Aneurysm and Dissection And/or Patent Ductus Arteriosus. Wiley, 2021.

MLA (8th ed.) Citation

Chesneau, Bertrand, et al. A +3 Variant at a Donor Splice Site Leads to a Skipping of the MYH11 Exon 32, a Recurrent RNA Defect Causing Heritable Thoracic Aortic Aneurysm and Dissection And/or Patent Ductus Arteriosus. Wiley, 2021.