000 01658 a2200517 4500
005 20250516130930.0
264 0 _c20140211
008 201402s 0 0 eng d
022 _a1872-6844
024 7 _a10.1016/j.eplepsyres.2012.11.004
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aMuhle, Hiltrud
245 0 0 _aThe role of SLC2A1 in early onset and childhood absence epilepsies.
_h[electronic resource]
260 _bEpilepsy research
_cJul 2013
300 _a229-33 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAdolescent
650 0 4 _aAge of Onset
650 0 4 _aBase Sequence
650 0 4 _aCohort Studies
650 0 4 _aEarly Diagnosis
650 0 4 _aEpilepsy, Absence
_xdiagnosis
650 0 4 _aFemale
650 0 4 _aGenetic Carrier Screening
650 0 4 _aGlucose Transporter Type 1
_xgenetics
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMolecular Sequence Data
650 0 4 _aMutation
_xgenetics
650 0 4 _aYoung Adult
700 1 _aHelbig, Ingo
700 1 _aFrøslev, Tobias Guldberg
700 1 _aSuls, Arvid
700 1 _avon Spiczak, Sarah
700 1 _aKlitten, Laura Line
700 1 _aDahl, Hans Atli
700 1 _aBrusgaard, Klaus
700 1 _aNeubauer, Bernd
700 1 _aDe Jonghe, Peter
700 1 _aTommerup, Niels
700 1 _aStephani, Ulrich
700 1 _aHjalgrim, Helle
700 1 _aMøller, Rikke Steensbjerre
773 0 _tEpilepsy research
_gvol. 105
_gno. 1-2
_gp. 229-33
856 4 0 _uhttps://doi.org/10.1016/j.eplepsyres.2012.11.004
_zAvailable from publisher's website
999 _c22409315
_d22409315