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Recurrent somatic mutations in ACVR1 in pediatric midline high-grade astrocytoma
- Fontebasso, Adam M;
- Papillon-Cavanagh, Simon;
- Schwartzentruber, Jeremy;
- Nikbakht, Hamid;
- Gerges, Noha;
- Fiset, Pierre-Olivier;
- Bechet, Denise;
- Faury, Damien;
- De Jay, Nicolas;
- Ramkissoon, Lori A;
- Corcoran, Aoife;
- Jones, David TW;
- Sturm, Dominik;
- Johann, Pascal;
- Tomita, Tadanori;
- Goldman, Stewart;
- Nagib, Mahmoud;
- Bendel, Anne;
- Goumnerova, Liliana;
- Bowers, Daniel C;
- Leonard, Jeffrey R;
- Rubin, Joshua B;
- Alden, Tord;
- Browd, Samuel;
- Geyer, J Russell;
- Leary, Sarah;
- Jallo, George;
- Cohen, Kenneth;
- Gupta, Nalin;
- Prados, Michael D;
- Carret, Anne-Sophie;
- Ellezam, Benjamin;
- Crevier, Louis;
- Klekner, Almos;
- Bognar, Laszlo;
- Hauser, Peter;
- Garami, Miklos;
- Myseros, John;
- Dong, Zhifeng;
- Siegel, Peter M;
- Malkin, Hayley;
- Ligon, Azra H;
- Albrecht, Steffen;
- Pfister, Stefan M;
- Ligon, Keith L;
- Majewski, Jacek;
- Jabado, Nada;
- Kieran, Mark W
Published Web Location
https://doi.org/10.1038/ng.2950Abstract
Nada Jabado and colleagues report identification of gain-of-function mutations in ACVR1, which encodes activin A receptor type I, in midline pediatric high-grade astrocytomas.
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