GLUT1 mutations are a rare cause of familial idiopathic generalized epilepsy

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GLUT1 mutations are a rare cause of familial idiopathic generalized epilepsy

Author: Striano, P.; Weber, Y. G.; Toliat, M. R.; Schubert, J.; Leu, C.; Chaimana, R.; Baulac, S.; Guerrero, R.; LeGuern, E.; Lehesjoki, A. -E.; Polvi, A.; Robbiano, A.; Serratosa, J. M.; Guerrini, R.; Nuernberg, P.; Sander, T.; Zara, F.; Lerche, H.; Marini, C.
Tübinger Autor(en):
Weber, Yvonne G.
Schubert, Julian
Lerche, Holger
Published in: Neurology (2012), Bd. 78, H. 8, S. 557-562
Verlagsangabe: Lippincott Williams & Wilkins
Language: English
Full text: http://dx.doi.org/10.1212/WNL.0b013e318247ff54
ISSN: 0028-3878
DDC Classifikation: 610 - Medicine and health
Dokumentart: Artikel
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