Exome-based Case-Control Study Identifies NOTCH1 Variants As the Major Monogenic Cause of CHD
Gregor Dombrowsky,Enrique Audain Martinez,Anna Wilsdon,Jeroen Breckpot,Alejandro Sifrim, Amilcar Perez-Riverol, Samira Hautmann,Anne-Karin Kahlert,Alex Postma,Connie R. Bezzina,Seema Mital,Robert Lesurf,Gillian Blue,David Winlaw,Sabine Klaassen,Felix Berger,Sven Dittrich,Brigitte Stiller,Hashim Abdul-Khaliq,Ingo Daehnert,Frances Bu'Lock,Thomas Pickardt,Ulrike Bauer,Hans-Heiner Kramer,Anselm Uebing,Siobhan Loughna,Matthew Hurles,Marc Phillip Hitz EUROPEAN JOURNAL OF HUMAN GENETICS（2024）
AI Read Science
Must-Reading Tree
Example
Generate MRT to find the research sequence of this paper