Phenotypic features of epilepsy due to sodium channelopathies – A single center experience from India

OBJECTIVES: Nearly 40% of pediatric epilepsies have a genetic basis. There is significant phenotypic and genotypic heterogeneity, especially in epilepsy syndromes caused by sodium channelopathies. Sodium channel subunit 1A (SCN1A)-related epilepsy represents the archetypical channel-associated gene...

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Detalles Bibliográficos
Autores principales: Viswanathan, Lakshminarayanapuram Gopal, Alapati, Sandhya, Nagappa, Madhu, Mundlamuri, Ravindranadh, Kenchaiah, Raghavendra, Asranna, Ajay, Padmanabha, Hansashree, Seshagiri, Doniparthi V., Sinha, Sanjib
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Scientific Scholar 2023
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10696347/
http://dx.doi.org/10.25259/JNRP_329_2023

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10696347/
http://dx.doi.org/10.25259/JNRP_329_2023

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