Novel Mutation Confirms Seizure Locus SCN1A is Also Familial Hemiplegic Migraine Locus FHM3

This publication has 18 references indexed in Scilit:

• Ion Channel Functional Candidate Genes in Multigenic Neuropsychiatric Disease
  Biological Psychiatry, 2006
• ATP1A2 : Un facteur essentiel dans la migraine hémiplégique familiale
  médecine/sciences, 2006
• Alterations in the α2 isoform of Na,K-ATPase associated with familial hemiplegic migraine type 2
  Proceedings of the National Academy of Sciences, 2005
• Gene dosage-dependent transmitter release changes at neuromuscular synapses of Cacna1a R192Q knockin mice are non-progressive and do not lead to morphological changes or muscle weakness
  Neuroscience, 2005
• Unraveling Monogenic Channelopathies and Their Implications for Complex Polygenic Disease
  American Journal of Human Genetics, 2003
• Sodium channels SCN1A, SCN2A and SCN3A in familial autism
  Molecular Psychiatry, 2003
• Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump α2 subunit associated with familial hemiplegic migraine type 2
  Nature Genetics, 2003
• Frequent mutations of SCN1A in severe myoclonic epilepsy in infancy
  Neurology, 2002
• Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel
  The Lancet, 2001
• Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2
  Nature Genetics, 2000