Linkage of Benign Familial Infantile Convulsions to Chromosome 16p12-q12 Suggests Allelism to the Infantile Convulsions and Choreoathetosis Syndrome
- 31 March 2001
- journal article
- research article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 68 (3) , 788-794
- https://doi.org/10.1086/318805
Abstract
No abstract availableKeywords
This publication has 33 references indexed in Scilit:
- Benign familial infantile convulsions: report of a UK family and confirmation of genetic heterogeneityJournal of Medical Genetics, 2000
- Benign Infantile Familial Convulsions: Natural History of a Case and Clinical Characteristics of a Large Italian FamilyNeuropediatrics, 1999
- Susceptibility Genes in Human EpilepsySeminars in Neurology, 1999
- Recent progress in the genetics of human epilepsiesneurogenetics, 1998
- Familial Infantile Convulsions and Paroxysmal Choreoathetosis: A New Neurological Syndrome Linked to the Pericentromeric Region of Human Chromosome 16American Journal of Human Genetics, 1997
- An Insertion Mutation of the CHRNA4 Gene in a Family With Autosomal Dominant Nocturnal Frontal Lobe EpilepsyHuman Molecular Genetics, 1997
- A missense mutation in the neuronal nicotinic acetylcholine receptor α4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsyNature Genetics, 1995
- Benign infantile epilepsy with autosomal dominant inheritanceBrain & Development, 1994
- Benign familial infantile epilepsyThe Journal of Pediatrics, 1993
- Benign infantile familial convulsionsEuropean Journal of Pediatrics, 1992