Common deletion variants causing protocadherin-α deficiency contribute to the complex genetics of BAV and left-sided congenital heart disease

Polakit Teekakirikul(Brigham and Women's Hospital), Cecilia Lo(University of Pittsburgh), Anastasia Miron(Hospital for Sick Children), Erik Fung(Chinese University of Hong Kong), Jianhua Xing(University of Pittsburgh), Yijen Wu(Children's Hospital of Pittsburgh), William A. Devine(University of Pittsburgh), Paul M. Kirshbom(Bon Secours Heart & Vascular Institute), Julie A. Phillippi(University of Pittsburgh), Anne Moreau de Bellaing(Délégation Paris 5), Marie Billaud(Harvard University), Leonid Emerel(University of Pittsburgh), Nathan Salamacha(University of Pittsburgh), Vidu Garg(The Ohio State University), Lisa J. Martin(Cincinnati Children's Hospital Medical Center), Samuel Wyman(University of Pittsburgh), Dennis M. McNamara(University of Pittsburgh Medical Center), Kim L. McBride(University of Calgary), Thomas G. Gleason(Asheville Cardiology Associates), William T. Mahle(Children's Center), Carrie B. Lee(University of North Carolina at Chapel Hill), Lazaros Kochilas(Emory Healthcare), George C. Gabriel(University of Pittsburgh), Wenjuan Zhu(Cardiovascular Institute of the South), Hung Sing Li(University of Pittsburgh), Abha Bais(University of Pittsburgh), Seema Mital(University of Toronto), Kylia Williams(University of Pittsburgh), Jiuann‐Huey Lin(University of Pittsburgh), Ankur Singh Saini(Hoshi University), Jonathan Klonowski(University of Pittsburgh), Cullen B. Young(University of Pittsburgh), Jennifer C. Hill(University of Pittsburgh), D. Woodrow Benson(University of Chicago Medical Center), Peter White(University of Pennsylvania), Jingyu Zhang(University of Pittsburgh), Jianbin Wang(King Center), Yihua He(Capital Medical University), Tara D. Richards(University of Pittsburgh), Tuantuan Tan(University of Pittsburgh), Michael Wang
Human Genetics and Genomics Advances
May 29, 2021
Cited by 15


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