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A +3 variant at a donor splice site leads to a skipping of ..:
Chesneau, Bertrand
;
Plancke, Aurélie
;
Rolland, Guillaume
...
Molecular Genetics & Genomic Medicine. 9 (2021) 11 - p. , 2021
Link:
https://doi.org/10.1002/mgg3.1814
RT Journal T1
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
UL https://suche.suub.uni-bremen.de/peid=cr-10.1002_mgg3.1814&Exemplar=1&LAN=DE A1 Chesneau, Bertrand A1 Plancke, Aurélie A1 Rolland, Guillaume A1 Marcheix, Bertrand A1 Dulac, Yves A1 Edouard, Thomas A1 Plaisancié, Julie A1 Aubert‐Mucca, Marion A1 Julia, Sophie A1 Langeois, Maud A1 Lavabre‐Bertrand, Thierry A1 Khau Van Kien, Philippe PB Wiley YR 2021 SN 2324-9269 SN 2324-9269 JF Molecular Genetics & Genomic Medicine VO 9 IS 11 LK http://dx.doi.org/https://doi.org/10.1002/mgg3.1814 DO https://doi.org/10.1002/mgg3.1814 SF ELIB - SuUB Bremen
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