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