| 000 | 01390 a2200457 4500 | ||
|---|---|---|---|
| 005 | 20250516223950.0 | ||
| 264 | 0 | _c20141103 | |
| 008 | 201411s 0 0 eng d | ||
| 022 | _a1528-1167 | ||
| 024 | 7 |
_a10.1111/epi.12715 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aAllen, Nicholas M | |
| 245 | 0 | 0 |
_aThe variable phenotypes of KCNQ-related epilepsy. _h[electronic resource] |
| 260 |
_bEpilepsia _cSep 2014 |
||
| 300 |
_ae99-105 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article | ||
| 650 | 0 | 4 |
_aBasal Ganglia _xpathology |
| 650 | 0 | 4 | _aChromosome Deletion |
| 650 | 0 | 4 |
_aChromosomes, Human, Pair 22 _xgenetics |
| 650 | 0 | 4 | _aElectroencephalography |
| 650 | 0 | 4 |
_aEpilepsy _xgenetics |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGenetic Association Studies |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 | _aInfant, Newborn |
| 650 | 0 | 4 |
_aKCNQ Potassium Channels _xgenetics |
| 650 | 0 | 4 | _aMagnetic Resonance Imaging |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aMutation _xgenetics |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 |
_aThalamus _xpathology |
| 700 | 1 | _aMannion, Maria | |
| 700 | 1 | _aConroy, Judith | |
| 700 | 1 | _aLynch, Sally A | |
| 700 | 1 | _aShahwan, Amre | |
| 700 | 1 | _aLynch, Bryan | |
| 700 | 1 | _aKing, Mary D | |
| 773 | 0 |
_tEpilepsia _gvol. 55 _gno. 9 _gp. e99-105 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1111/epi.12715 _zAvailable from publisher's website |
| 999 |
_c24034025 _d24034025 |
||