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CCDC88C variants are associated with focal epilepsy and genotype-phenotype correlation.
Clin Genet. 2024 Apr;105(4):397-405. doi: 10.1111/cge.14476. Epub 2024 Jan 3.
Clin Genet. 2024.
PMID: 38173219
Association of LONP1 gene with epilepsy and the sub-regional effect.
Li SX, He N, Liao JX, Lu XG, Hu WG, Liu XR, Liao WP, Song XW, Li B.
Li SX, et al.
Sci Rep. 2024 Oct 26;14(1):25575. doi: 10.1038/s41598-024-77039-9.
Sci Rep. 2024.
PMID: 39462050
Free PMC article.
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ARHGAP4 variants are associated with X-linked early-onset temporal lobe epilepsy.
Hu YY, Song W, Liu ZG, Ye XG, Zhang HW, Li X, Luo JX, Wang PY, Wang J, Lin XF, Zhu HL, Liao WP, Li B, Chen XQ.
Hu YY, et al.
World J Pediatr. 2024 Aug;20(8):859-867. doi: 10.1007/s12519-024-00830-1. Epub 2024 Jul 26.
World J Pediatr. 2024.
PMID: 39060771
No abstract available.
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