Truncating mutation in TANC2 in a Chinese boy associated with Lennox-Gastaut syndrome: a case report

Truncating mutation in TANC2 in a Chinese boy associated with Lennox-Gastaut syndrome: a case report

Abstract Background Lennox-Gastaut syndrome (LGS) is a severe epileptic encephalopathy that can be caused by brain malformations or genetic mutations. Recently, genome-wide association studies have led to the identification of novel mutations associated with LGS. The TANC2 gene, encodes a synaptic s...

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Bibliographic Details
Main Authors: Yang Tian, Zhen Shi, Chi Hou, Wenjuan Li, Xiuying Wang, Haixia Zhu, Xiaojing Li, Wen-Xiong Chen
Format: Article
Language:English
Published: BMC 2021-12-01
Series:BMC Pediatrics
Subjects:
TANC2
Epilepsy
Lennox-Gastaut syndrome
Case report
Online Access:https://doi.org/10.1186/s12887-021-03021-3

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