McLellan, Ailsa <br/><br/>
Phenotypic comparison of two Scottish families with mutations in different genes causing autosomal dominant nocturnal frontal lobe epilepsy.  [electronic resource] 

 -  Epilepsia  Apr 2003 
 - 613-7 p.  digital 
<br/><br/> Publication Type: Comparative Study; Journal Article 
<br/><br/><label>ISSN: </label>0013-9580 
<br/><br/><label>Standard No.: </label>10.1046/j.1528-1157.2003.20102.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Aged<br/>Aged, 80 and over<br/>Alleles<br/>Chromosome Aberrations<br/>Comorbidity<br/>DNA Mutational Analysis<br/>Epilepsy, Frontal Lobe--diagnosis<br/>Female<br/>Gene Frequency--genetics<br/>Genes, Dominant--genetics<br/>Genetic Markers--genetics<br/>Genetic Predisposition to Disease--genetics<br/>Haplotypes--genetics<br/>Humans<br/>Male<br/>Mental Disorders--diagnosis<br/>Middle Aged<br/>Pedigree<br/>Phenotype<br/>Receptors, Nicotinic--genetics<br/>Scotland