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

Wu, Yi; Wu, Dan; Lan, Yulong; Lan, Shaocong; Li, Duo; Zheng, Zexin; Wang, Hongwu; Ma, Lian.

Afiliação

Wu Y; Department of Pediatrics, Second Affiliated Hospital of Shantou University Medical College, Shantou, China.
Wu D; Department of Pediatrics, Second Affiliated Hospital of Shantou University Medical College, Shantou, China.
Lan Y; Centre for Precision Health, School of Medical and Health Sciences, Edith Cowan University, Joondalup, WA, Australia.
Lan S; Centre for Precision Health, School of Medical and Health Sciences, Edith Cowan University, Joondalup, WA, Australia.
Li D; Department of Cardiology, Second Affiliated Hospital of Shantou University Medical College, Shantou, China.
Zheng Z; Department of clinical Medicine, Guangdong Medical University, Zhanjiang, China.
Wang H; Department of Pediatrics, Second Affiliated Hospital of Shantou University Medical College, Shantou, China.
Ma L; Department of Pediatrics, Second Affiliated Hospital of Shantou University Medical College, Shantou, China.

Front Genet ; 14: 1025390, 2023.

Article em En | MEDLINE | ID: mdl-37347056