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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...
| Autores principales: | , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Frontiers Media S.A.
2023
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| Materias: | |
| 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 |