Rare and de novo variants in 827 congenital diaphragmatic hernia probands implicate LONP1 as candidate risk gene
Title:
Rare and de novo variants in 827 congenital diaphragmatic hernia probands implicate LONP1 as candidate risk gene
Author:
Qiao, Lu Xu, Le Yu, Lan Wynn, Julia Hernan, Rebecca Zhou, Xueya Farkouh-Karoleski, Christiana Krishnan, Usha S. Khlevner, Julie De, Aliva Zygmunt, Annette Crombleholme, Timothy Lim, Foong-Yen Needelman, Howard Cusick, Robert A. Mychaliska, George B. Warner, Brad W. Wagner, Amy J. Danko, Melissa E. Chung, Dai Potoka, Douglas KosiĆski, Przemyslaw McCulley, David J. Elfiky, Mahmoud Azarow, Kenneth Fialkowski, Elizabeth Schindel, David Soffer, Samuel Z. Lyon, Jane B. Zalieckas, Jill M. Vardarajan, Badri N. Aspelund, Gudrun Duron, Vincent P. High, Frances A. Sun, Xin Donahoe, Patricia K. Shen, Yufeng Chung, Wendy K.