KCC2 rs2297201 Gene Polymorphism Might be a Predictive Genetic Marker of Febrile Seizures

Introduction: Febrile seizures (FS) are the most common neurological disease in childhood. The etiology of FS is the subject of numerous studies including studies regarding genetic predisposition. Aim: The aim of the study was to analyze the association of TRPV1 rs222747 and KCC2 rs2297201 gene poly...

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Detalles Bibliográficos
Autores principales: Dimitrijevic, Sanja, Jekic, Biljana, Cvjeticanin, Suzana, Tucovic, Aleksandra, Filipovic, Tamara, Novaković, Ivana, Ivić, Bojana, Nikolic, Dimitrije
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Original Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9016559/
https://www.ncbi.nlm.nih.gov/pubmed/35414199
http://dx.doi.org/10.1177/17590914221093257

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9016559/
https://www.ncbi.nlm.nih.gov/pubmed/35414199
http://dx.doi.org/10.1177/17590914221093257

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