Molecular genetics of infantile nervous system channelopathies

This publication has 27 references indexed in Scilit:

• From molecule to malady
  Nature, 2006
• Mutations of Neuronal Voltage‐gated Na⁺ Channel α1 Subunit Gene SCN1A in Core Severe Myoclonic Epilepsy in Infancy (SMEI) and in Borderline SMEI (SMEB)
  Epilepsia, 2004
• Mutations of sodium channel alpha subunit type 1 (SCN1A) in intractable childhood epilepsies with frequent generalized tonic-clonic seizures
  Brain, 2003
• Truncation of the GABAA-Receptor γ2 Subunit in a Family with Generalized Epilepsy with Febrile Seizures Plus
  The American Journal of Human Genetics, 2002
• De Novo Mutations in the Sodium-Channel Gene SCN1A Cause Severe Myoclonic Epilepsy of Infancy
  The American Journal of Human Genetics, 2001
• Neuronal Sodium-Channel α1-Subunit Mutations in Generalized Epilepsy with Febrile Seizures Plus
  The American Journal of Human Genetics, 2001
• Radicals r'aging
  Nature Genetics, 1998
• A Potassium Channel Mutation in Neonatal Human Epilepsy
  Science, 1998
• A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family
  Nature Genetics, 1998
• A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns
  Nature Genetics, 1998