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Case report: Sex-specific characteristics of epilepsy phenotypes associated with Xp22.31 deletion: a case report and review

Deletion in the Xp22.31 region is increasingly suggested to be involved in the etiology of epilepsy. Little is known regarding the genomic and clinical delineations of X-linked epilepsy in the Chinese population or the sex-stratified difference in epilepsy characteristics associated with deletions i...

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Detalles Bibliográficos
Autores principales:	Wu, Yi, Wu, Dan, Lan, Yulong, Lan, Shaocong, Li, Duo, Zheng, Zexin, Wang, Hongwu, Ma, Lian
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2023
Materias:	Genetics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10280017/ https://www.ncbi.nlm.nih.gov/pubmed/37347056 http://dx.doi.org/10.3389/fgene.2023.1025390

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