Phenotypic comparison of two Scottish families with mutations in different genes causing autosomal dominant nocturnal frontal lobe epilepsy.

Epilepsia

Volumn 44, Issue 4, 2003, Pages 613-617

  McLellan, Ailsa ^a   Phillips, Hilary A ^a   Rittey, Christopher ^a   Kirkpatrick, Martin ^a   Mulley, John C ^a   Goudie, David ^a   Stephenson, John B P ^a   Tolmie, John ^a   Scheffer, Ingrid E ^a   Berkovic, Samuel F ^a   Zuberi, Sameer M ^a  

^a UNIVERSITY OF DUNDEE   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

CHRNB2 PROTEIN, HUMAN; NICOTINIC ACETYLCHOLINE RECEPTOR ALPHA4 SUBUNIT; NICOTINIC RECEPTOR;

ADOLESCENT; ADULT; AGED; ALLELE; ARTICLE; CHROMOSOME ABERRATION; COMORBIDITY; COMPARATIVE STUDY; DOMINANT GENE; FEMALE; FRONTAL LOBE EPILEPSY; GENE FREQUENCY; GENETIC MARKER; GENETIC PREDISPOSITION; GENETICS; HAPLOTYPE; HUMAN; MALE; MENTAL DISEASE; MIDDLE AGED; NUCLEOTIDE SEQUENCE; PEDIGREE; PHENOTYPE; UNITED KINGDOM;

ADOLESCENT; ADULT; AGED; AGED, 80 AND OVER; ALLELES; CHROMOSOME ABERRATIONS; COMORBIDITY; DNA MUTATIONAL ANALYSIS; EPILEPSY, FRONTAL LOBE; FEMALE; GENE FREQUENCY; GENES, DOMINANT; GENETIC MARKERS; GENETIC PREDISPOSITION TO DISEASE; HAPLOTYPES; HUMANS; MALE; MENTAL DISORDERS; MIDDLE AGED; PEDIGREE; PHENOTYPE; RECEPTORS, NICOTINIC; SCOTLAND;

EID: 0042878437     PISSN: 00139580     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1528-1157.2003.20102.x     Document Type: Article

References (0)