000 | 01888 a2200589 4500 | ||
---|---|---|---|
005 | 20250514063720.0 | ||
264 | 0 | _c20030909 | |
008 | 200309s 0 0 eng d | ||
022 | _a0013-9580 | ||
024 | 7 |
_a10.1046/j.1528-1157.2003.20102.x _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aMcLellan, Ailsa | |
245 | 0 | 0 |
_aPhenotypic comparison of two Scottish families with mutations in different genes causing autosomal dominant nocturnal frontal lobe epilepsy. _h[electronic resource] |
260 |
_bEpilepsia _cApr 2003 |
||
300 |
_a613-7 p. _bdigital |
||
500 | _aPublication Type: Comparative Study; Journal Article | ||
650 | 0 | 4 | _aAdolescent |
650 | 0 | 4 | _aAdult |
650 | 0 | 4 | _aAged |
650 | 0 | 4 | _aAged, 80 and over |
650 | 0 | 4 | _aAlleles |
650 | 0 | 4 | _aChromosome Aberrations |
650 | 0 | 4 | _aComorbidity |
650 | 0 | 4 | _aDNA Mutational Analysis |
650 | 0 | 4 |
_aEpilepsy, Frontal Lobe _xdiagnosis |
650 | 0 | 4 | _aFemale |
650 | 0 | 4 |
_aGene Frequency _xgenetics |
650 | 0 | 4 |
_aGenes, Dominant _xgenetics |
650 | 0 | 4 |
_aGenetic Markers _xgenetics |
650 | 0 | 4 |
_aGenetic Predisposition to Disease _xgenetics |
650 | 0 | 4 |
_aHaplotypes _xgenetics |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aMale |
650 | 0 | 4 |
_aMental Disorders _xdiagnosis |
650 | 0 | 4 | _aMiddle Aged |
650 | 0 | 4 | _aPedigree |
650 | 0 | 4 | _aPhenotype |
650 | 0 | 4 |
_aReceptors, Nicotinic _xgenetics |
650 | 0 | 4 | _aScotland |
700 | 1 | _aPhillips, Hilary A | |
700 | 1 | _aRittey, Christopher | |
700 | 1 | _aKirkpatrick, Martin | |
700 | 1 | _aMulley, John C | |
700 | 1 | _aGoudie, David | |
700 | 1 | _aStephenson, John B P | |
700 | 1 | _aTolmie, John | |
700 | 1 | _aScheffer, Ingrid E | |
700 | 1 | _aBerkovic, Samuel F | |
700 | 1 | _aZuberi, Sameer M | |
773 | 0 |
_tEpilepsia _gvol. 44 _gno. 4 _gp. 613-7 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1046/j.1528-1157.2003.20102.x _zAvailable from publisher's website |
999 |
_c12473586 _d12473586 |