Benign infantile familial convulsions are not an allelic form of the benign familial neonatal convulsions gene

Annals of Neurology

Volumn 35, Issue 4, 1994, Pages 479-482

  Malafosse, A ^a   Beck, C ^a   Bellet, H ^a   Di Capua, M ^b   Dulac, O ^c   Echenne, B ^d   Fusco, L ^b   Lucchini, P ^e   Ricci, S ^b   Sebastianelli, R ^b   Feingold, J ^a   Baldy Moulinier M ^a   Vigevano, F ^b  

^a INSERM   (France)

^b BAMBINO GESÙ CHILDREN S HOSPITAL   (Italy)

^c HÔPITAL SAINT VINCENT DE PAUL   (France)

^d GUI DE CHAULIAC HOSPITAL   (France)

^e GENERAL HOSPITAL   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ALLELE; ARTICLE; CHROMOSOME 20Q; CONVULSION; CROSSING OVER; FAMILIAL DISEASE; FEMALE; GENETIC LINKAGE; HUMAN; HUMAN CELL; INFANT; INFANT DISEASE; MAJOR CLINICAL STUDY; MALE; NEWBORN; NEWBORN DISEASE; ONSET AGE; PEDIGREE; PRIORITY JOURNAL;

AGE OF ONSET; ALLELES; CHILD, PRESCHOOL; DNA; FEMALE; HUMANS; LINKAGE (GENETICS); LOD SCORE; MALE; PEDIGREE; SEIZURES;

EID: 0028231357     PISSN: 03645134     EISSN: 15318249     Source Type: Journal    
DOI: 10.1002/ana.410350417     Document Type: Article

References (12)

1. Genes and epilepsy
2. Commission on Classification and Terminology of the International League Against Epilepsy. Proposal for revised classification of epilepsies and epileptic syndromes
3. Benign neonatal convulsions
4. Benign infantile familial convulsions
5. Benign familial neonatal convulsions linked to genetic markers on chromosome 20
6. Benign familial neonatal convulsions: evidence for clinical and genetic heterogeneity
7. Confirmation of linkage of benign neonatal convulsions to D20S19 and D20S20
8. Use of cyclosporin A in establishing Epstein‐Barr virus transformed human lymphoblastoid cell lines
9. Multilocus linkage analysis in humans: detection of linkage and estimation of recombination
10. Convulsioni infantili familiari benigne
11. Electroclinical signs of benign neonatal familial convulsions