Associated Papers
SCN9A should not be considered an epilepsy gene; Refuting a gene-disease association.
Ghanty I et al.
Epilepsia, 2025
No association between SCN9A and monogenic human epilepsy disorders.
Fasham J et al.
Plos Genetics, 2020
Novel mutation of SCN9A gene causing generalized epilepsy with febrile seizures plus in a Chinese family.
Zhang T et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2020
Genetic epilepsy with febrile seizures plus: Refining the spectrum.
Zhang YH et al.
Neurology, 2017
Short-lasting unilateral neuralgiform headache attacks with ispilateral facial flushing is a new variant of paroxysmal extreme pain disorder.
Imai N et al.
The Journal of Headache and Pain, 2015
Role of the sodium channel SCN9A in genetic epilepsy with febrile seizures plus and Dravet syndrome.
Mulley JC et al.
Epilepsia, 2013
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