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Common deletion variants causing protocadherin-α deficiency..:
Polakit Teekakirikul
;
Wenjuan Zhu
;
George C. Gabriel
...
http://www.sciencedirect.com/science/article/pii/S266624772100018X. , 2021
Link:
https://doi.org/10.1016/j.xhgg.2021.100037
RT Journal T1
Common deletion variants causing protocadherin-α deficiency contribute to the complex genetics of BAV and left-sided congenital heart disease
UL https://suche.suub.uni-bremen.de/peid=base-ftdoajarticles:oai:doaj.org_article:0b7019f7bd454037bec2471ea5feef8c&Exemplar=1&LAN=DE A1 Polakit Teekakirikul A1 Wenjuan Zhu A1 George C. Gabriel A1 Cullen B. Young A1 Kylia Williams A1 Lisa J. Martin A1 Jennifer C. Hill A1 Tara Richards A1 Marie Billaud A1 Julie A. Phillippi A1 Jianbin Wang A1 Yijen Wu A1 Tuantuan Tan A1 William Devine A1 Jiuann-huey Lin A1 Abha S. Bais A1 Jonathan Klonowski A1 Anne Moreau de Bellaing A1 Ankur Saini A1 Michael X. Wang A1 Leonid Emerel A1 Nathan Salamacha A1 Samuel K. Wyman A1 Carrie Lee A1 Hung Sing Li A1 Anastasia Miron A1 Jingyu Zhang A1 Jianhua Xing A1 Dennis M. McNamara A1 Erik Fung A1 Paul Kirshbom A1 William Mahle A1 Lazaros K. Kochilas A1 Yihua He A1 Vidu Garg A1 Peter White A1 Kim L. McBride A1 D. Woodrow Benson A1 Thomas G. Gleason A1 Seema Mital A1 Cecilia W. Lo PB Elsevier YR 2021 K1 bicuspid aortic valve K1 coarctaction K1 left ventricular outflow obstruction K1 genetics K1 protocadherin K1 copy number variants K1 QH426-470 JF http://www.sciencedirect.com/science/article/pii/S266624772100018X LK http://dx.doi.org/https://doi.org/10.1016/j.xhgg.2021.100037 DO https://doi.org/10.1016/j.xhgg.2021.100037 SF ELIB - SuUB Bremen
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