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
2004 ◽
Vol 12
(3)
◽
pp. 173-180
◽
2013 ◽
Vol 22
(4)
◽
pp. 498-498
Keyword(s):
1998 ◽
Vol 31
(2)
◽
pp. 153A
Keyword(s):