Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis

✍ Scribed by Sharma, Vikram P; Fenwick, Aimée L; Brockop, Mia S; McGowan, Simon J; Goos, Jacqueline A C; Hoogeboom, A Jeannette M; Brady, Angela F; Jeelani, Nu Owase; Lynch, Sally Ann; Mulliken, John B; Murray, Dylan J; Phipps, Julie M; Sweeney, Elizabeth; Tomkins, Susan E; Wilson, Louise C; Bennett, Sophia; Cornall, Richard J; Broxholme, John; Kanapin, Alexander; Johnson, David; Wall, Steven A; van der Spek, Peter J; Mathijssen, Irene M J; Maxson, Robert E; Twigg, Stephen R F; Wilkie, Andrew O M

• Book ID: 121188692
• Publisher: Nature Publishing Group
• Year: 2013
• Tongue: English
• Weight: 833 KB
• Volume: 45
• Category: Article
• ISSN: 1061-4036
• DOI: 10.1038/ng.2531