000 01737 a2200517 4500
005 20250515161857.0
264 0 _c20090714
008 200907s 0 0 eng d
022 _a1460-2083
024 7 _a10.1093/hmg/ddp081
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aPapale, Ligia A
245 0 0 _aHeterozygous mutations of the voltage-gated sodium channel SCN8A are associated with spike-wave discharges and absence epilepsy in mice.
_h[electronic resource]
260 _bHuman molecular genetics
_cMay 2009
300 _a1633-41 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
650 0 4 _aAnimals
650 0 4 _aBase Sequence
650 0 4 _aDisease Models, Animal
650 0 4 _aElectrophysiology
650 0 4 _aEpilepsy, Absence
_xgenetics
650 0 4 _aHeterozygote
650 0 4 _aHumans
650 0 4 _aMice
650 0 4 _aMice, Inbred C3H
650 0 4 _aMice, Inbred C57BL
650 0 4 _aMice, Transgenic
650 0 4 _aMolecular Sequence Data
650 0 4 _aMutation
650 0 4 _aMutation, Missense
650 0 4 _aNAV1.6 Voltage-Gated Sodium Channel
650 0 4 _aNerve Tissue Proteins
_xgenetics
650 0 4 _aPhenotype
650 0 4 _aSodium Channels
_xgenetics
700 1 _aBeyer, Barbara
700 1 _aJones, Julie M
700 1 _aSharkey, Lisa M
700 1 _aTufik, Sergio
700 1 _aEpstein, Michael
700 1 _aLetts, Verity A
700 1 _aMeisler, Miriam H
700 1 _aFrankel, Wayne N
700 1 _aEscayg, Andrew
773 0 _tHuman molecular genetics
_gvol. 18
_gno. 9
_gp. 1633-41
856 4 0 _uhttps://doi.org/10.1093/hmg/ddp081
_zAvailable from publisher's website
999 _c18695971
_d18695971