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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