Failure to replicate association between the gene for the neuronal nicotinic acetylcholine receptor ?4 subunit (CHRNA4) and IGE

This publication has 9 references indexed in Scilit:

• Epilepsies in twins: Genetics of the major epilepsy syndromes
  Annals of Neurology, 1998
• A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns
  Nature Genetics, 1998
• Possible association of a silent polymorphism in the neuronal nicotinic acetylcholine receptor subunit α4 with common idiopathic generalized epilepsies
  American Journal of Medical Genetics, 1997
• An Insertion Mutation of the CHRNA4 Gene in a Family With Autosomal Dominant Nocturnal Frontal Lobe Epilepsy
  Human Molecular Genetics, 1997
• A missense mutation in the neuronal nicotinic acetylcholine receptor α4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy
  Nature Genetics, 1995
• A Haplotype-Based Haplotype Relative Risk’ Approach to Detecting Allelic Associations
  Human Heredity, 1992
• Proposal for Revised Classification of Epilepsies and Epileptic Syndromes
  Epilepsia, 1989
• Morbidity Risk for Seizures and Epilepsy in Offspring of Patients with Epilepsy
  Published by Springer Nature ,1989
• Essential Isochronic Epilepsy in MZ Twin Pairs
  Acta geneticae medicae et gemellologiae, 1971