A case of genetic epilepsy with febrile seizures plus caused by dual variations in GABRG2 and SCN1A and a genotype-phenotype study of the family
Objective To investigate the phenotypic impact of dual variations in GABRG2 and SCN1A on genetic epilepsy with febrile seizures plus (GEFS+). Methods The clinical data of a 3-year-old girl and her three generations of family members who visited the Pediatric Internal Medicine Department due to "repe...
Gorde:
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| Formatua: | Artigo |
| Hizkuntza: | Chinês |
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Editorial Office of Journal of Clinical Pediatrics
2026-01-01
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| Saila: | Linchuang erke zazhi |
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| Sarrera elektronikoa: | https://jcp.xinhuamed.com.cn/fileup/1000-3606/PDF/1767591125376-2108603087.pdf |
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