000 | 02891 a2200913 4500 | ||
---|---|---|---|
005 | 20250518085600.0 | ||
264 | 0 | _c20201019 | |
008 | 202010s 0 0 eng d | ||
022 | _a1528-1167 | ||
024 | 7 |
_a10.1111/epi.16438 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aBrunklaus, Andreas | |
245 | 0 | 0 |
_aBiological concepts in human sodium channel epilepsies and their relevance in clinical practice. _h[electronic resource] |
260 |
_bEpilepsia _c03 2020 |
||
300 |
_a387-399 p. _bdigital |
||
500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
650 | 0 | 4 | _aAge of Onset |
650 | 0 | 4 |
_aAutism Spectrum Disorder _xgenetics |
650 | 0 | 4 | _aChild |
650 | 0 | 4 | _aChild, Preschool |
650 | 0 | 4 | _aCodon, Nonsense |
650 | 0 | 4 | _aDNA Copy Number Variations |
650 | 0 | 4 | _aElectroencephalography |
650 | 0 | 4 |
_aEpileptic Syndromes _xdrug therapy |
650 | 0 | 4 | _aFemale |
650 | 0 | 4 | _aGain of Function Mutation |
650 | 0 | 4 | _aGene Deletion |
650 | 0 | 4 | _aGene Duplication |
650 | 0 | 4 | _aGene Expression |
650 | 0 | 4 | _aGene Expression Regulation, Developmental |
650 | 0 | 4 | _aGenotype |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aInfant |
650 | 0 | 4 | _aInfant, Newborn |
650 | 0 | 4 | _aLoss of Function Mutation |
650 | 0 | 4 | _aMale |
650 | 0 | 4 | _aMutation, Missense |
650 | 0 | 4 |
_aNAV1.1 Voltage-Gated Sodium Channel _xgenetics |
650 | 0 | 4 |
_aNAV1.2 Voltage-Gated Sodium Channel _xgenetics |
650 | 0 | 4 |
_aNAV1.3 Voltage-Gated Sodium Channel _xgenetics |
650 | 0 | 4 |
_aNAV1.6 Voltage-Gated Sodium Channel _xgenetics |
650 | 0 | 4 |
_aNeurodevelopmental Disorders _xgenetics |
650 | 0 | 4 | _aPhenotype |
650 | 0 | 4 |
_aSodium Channel Blockers _xtherapeutic use |
650 | 0 | 4 |
_aSodium Channels _xgenetics |
700 | 1 | _aDu, Juanjiangmeng | |
700 | 1 | _aSteckler, Felix | |
700 | 1 | _aGhanty, Ismael I | |
700 | 1 | _aJohannesen, Katrine M | |
700 | 1 | _aFenger, Christina Dühring | |
700 | 1 | _aSchorge, Stephanie | |
700 | 1 | _aBaez-Nieto, David | |
700 | 1 | _aWang, Hao-Ran | |
700 | 1 | _aAllen, Andrew | |
700 | 1 | _aPan, Jen Q | |
700 | 1 | _aLerche, Holger | |
700 | 1 | _aHeyne, Henrike | |
700 | 1 | _aSymonds, Joseph D | |
700 | 1 | _aZuberi, Sameer M | |
700 | 1 | _aSanders, Stephan | |
700 | 1 | _aSheidley, Beth R | |
700 | 1 | _aCraiu, Dana | |
700 | 1 | _aOlson, Heather E | |
700 | 1 | _aWeckhuysen, Sarah | |
700 | 1 | _aDeJonge, Peter | |
700 | 1 | _aHelbig, Ingo | |
700 | 1 | _aVan Esch, Hilde | |
700 | 1 | _aBusa, Tiffany | |
700 | 1 | _aMilh, Matthieu | |
700 | 1 | _aIsidor, Bertrand | |
700 | 1 | _aDepienne, Christel | |
700 | 1 | _aPoduri, Annapurna | |
700 | 1 | _aCampbell, Arthur J | |
700 | 1 | _aDimidschstein, Jordane | |
700 | 1 | _aMøller, Rikke S | |
700 | 1 | _aLal, Dennis | |
773 | 0 |
_tEpilepsia _gvol. 61 _gno. 3 _gp. 387-399 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1111/epi.16438 _zAvailable from publisher's website |
999 |
_c30665428 _d30665428 |