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

por Teekakirikul, Polakit, Zhu, Wenjuan, Gabriel, George C., Young, Cullen B., Williams, Kylia, Martin, Lisa J., Hill, Jennifer C., Richards, Tara, Billaud, Marie, Phillippi, Julie A., Wang, Jianbin, Wu, Yijen, Tan, Tuantuan, Devine, William, Lin, Jiuann-huey, Bais, Abha S., Klonowski, Jonathan, de Bellaing, Anne Moreau, Saini, Ankur, Wang, Michael X., Emerel, Leonid, Salamacha, Nathan, Wyman, Samuel K., Lee, Carrie, Li, Hung Sing, Miron, Anastasia, Zhang, Jingyu, Xing, Jianhua, McNamara, Dennis M., Fung, Erik, Kirshbom, Paul, Mahle, William, Kochilas, Lazaros K., He, Yihua, Garg, Vidu, White, Peter, McBride, Kim L., Benson, D. Woodrow, Gleason, Thomas G., Mital, Seema, Lo, Cecilia W.
Publicado 2021