| 000 | 01893 a2200577 4500 | ||
|---|---|---|---|
| 005 | 20250517050140.0 | ||
| 264 | 0 | _c20151216 | |
| 008 | 201512s 0 0 eng d | ||
| 022 | _a1526-632X | ||
| 024 | 7 |
_a10.1212/WNL.0000000000001926 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aHowell, Katherine B | |
| 245 | 0 | 0 |
_aSCN2A encephalopathy: A major cause of epilepsy of infancy with migrating focal seizures. _h[electronic resource] |
| 260 |
_bNeurology _cSep 2015 |
||
| 300 |
_a958-66 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 |
_aBrain Diseases _xcomplications |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 |
_aElectroencephalography _xmethods |
| 650 | 0 | 4 |
_aEpilepsies, Partial _xcomplications |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGenetic Predisposition to Disease |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aMutation _xgenetics |
| 650 | 0 | 4 |
_aNAV1.2 Voltage-Gated Sodium Channel _xgenetics |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 |
_aSeizures _xcomplications |
| 650 | 0 | 4 |
_aSpasms, Infantile _xgenetics |
| 650 | 0 | 4 | _aYoung Adult |
| 700 | 1 | _aMcMahon, Jacinta M | |
| 700 | 1 | _aCarvill, Gemma L | |
| 700 | 1 | _aTambunan, Dimira | |
| 700 | 1 | _aMackay, Mark T | |
| 700 | 1 | _aRodriguez-Casero, Victoria | |
| 700 | 1 | _aWebster, Richard | |
| 700 | 1 | _aClark, Damian | |
| 700 | 1 | _aFreeman, Jeremy L | |
| 700 | 1 | _aCalvert, Sophie | |
| 700 | 1 | _aOlson, Heather E | |
| 700 | 1 | _aMandelstam, Simone | |
| 700 | 1 | _aPoduri, Annapurna | |
| 700 | 1 | _aMefford, Heather C | |
| 700 | 1 | _aHarvey, A Simon | |
| 700 | 1 | _aScheffer, Ingrid E | |
| 773 | 0 |
_tNeurology _gvol. 85 _gno. 11 _gp. 958-66 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1212/WNL.0000000000001926 _zAvailable from publisher's website |
| 999 |
_c25186521 _d25186521 |
||