One platform for all researcher needs
AI-powered academic writing assistant
Your #1 AI companion for literature search
AI tool for graphics, illustrations, and artwork
Unlock unlimited use of all AI tools with the Editage All Access membership.
Explore Editage All Access
Open Accesshttps://doi.org/10.1136/jmedgenet-2013-102248
Copy DOI Journal: Journal of Medical Genetics |  Publication Date: Apr 8, 2014 |
 Citations: 82 |
Affiliation: Max Planck Institute for Molecular Genetics, Charité - Universitätsmedizin Berlin, Royal Children's Hospital, Lund University, KU Leuven, University Children's Hospital Zurich, Kinderkrankenhaus auf der Bult, University of Göttingen, Innsbruck Medical University, Universität Innsbruck, University Hospital Heidelberg, Heidelberg University, John Hunter Children's Hospital, German Center for Lung Research, Medical University of Sofia, National Institute of Neurological Disorders and StrokeBackgroundNKX2-1 encodes a transcription factor with large impact on the development of brain, lung and thyroid. Germline mutations of NKX2-1 can lead to dysfunction and malformations of these organs. Starting...
Sign-in/Register to access full text options 
Free) Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call
