GLUT1 mutations are a rare cause of familial idiopathic generalized epilepsy.
dc.contributor.author | Striano, P | |
dc.contributor.author | Weber, YG | |
dc.contributor.author | Toliat, MR | |
dc.contributor.author | Schubert, J | |
dc.contributor.author | Leu, C | |
dc.contributor.author | Chaimana, R | |
dc.contributor.author | Baulac, S | |
dc.contributor.author | Guerrero, R | |
dc.contributor.author | LeGuern, E | |
dc.contributor.author | Lehesjoki, AE | |
dc.contributor.author | Polvi, A | |
dc.contributor.author | Robbiano, A | |
dc.contributor.author | Serratosa, JM | |
dc.contributor.author | Guerrini, R | |
dc.contributor.author | Nürnberg, P | |
dc.contributor.author | Sander, T | |
dc.contributor.author | Zara, F | |
dc.contributor.author | Lerche, H | |
dc.contributor.author | Marini, C | |
dc.contributor.author | EPICURE, Consortium. | |
dc.date.accessioned | 2021-03-02T22:56:36Z | |
dc.date.available | 2021-03-02T22:56:36Z | |
dc.identifier.citation | Striano P., Weber Y., Toliat M., Schubert J., Leu C., Chaimana R., Baulac S., Guerrero R., LeGuern E., Lehesjoki A., et al., "GLUT1 mutations are a rare cause of familial idiopathic generalized epilepsy.", Neurology, cilt.78, ss.557-62, 2012 | |
dc.identifier.issn | 0028-3878 | |
dc.identifier.other | vv_1032021 | |
dc.identifier.other | av_0f88701d-bb59-4fc5-8cb2-cc5a761a1cad | |
dc.identifier.uri | http://hdl.handle.net/20.500.12627/15981 | |
dc.identifier.uri | https://doi.org/10.1212/wnl.0b013e318247ff54 | |
dc.language.iso | eng | |
dc.title | GLUT1 mutations are a rare cause of familial idiopathic generalized epilepsy. | |
dc.type | Makale | |
dc.relation.journal | Neurology | |
dc.contributor.department | , , | |
dc.identifier.volume | 78 | |
dc.identifier.startpage | 557 | |
dc.identifier.endpage | 62 | |
dc.contributor.firstauthorID | 733756 |
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