The role of SLC2A1 mutations in myoclonic astatic epilepsy and absence epilepsy, and the estimated frequency of GLUT1 deficiency syndrome. (Q41149745)
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scientific article published on 5 November 2015
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | The role of SLC2A1 mutations in myoclonic astatic epilepsy and absence epilepsy, and the estimated frequency of GLUT1 deficiency syndrome. |
scientific article published on 5 November 2015 |
Statements
The role of SLC2A1 mutations in myoclonic astatic epilepsy and absence epilepsy, and the estimated frequency of GLUT1 deficiency syndrome (English)
Renzo Guerrini
Jan Larsen
Katrine Marie Johannesen
Jakob Ek
Shan Tang
Carla Marini
Susanne Blichfeldt
Maria Kibaek
Sarah von Spiczak
Mimoza Frangu
Bernd Axel Neubauer
Peter Uldall
MAE working group of EuroEPINOMICS RES Consortium
Rebecca Kleiss
Hiltrud Muhle
Marina Nikanorova
Birgit Jepsen
Ulrich Stephani
Morten Duno
Helle Hjalgrim
Deb Pal
Ingo Helbig
Sarah Weckhuysen
5 November 2015
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