| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 8681255 | Brain and Development | 2018 | 6 Pages |
Abstract
GRIN2A mutation is a genetic cause in less than 11% patients with LKS or ABPE. GRIN2A gene is a rare causative gene in Chinese patients with EAS, suggesting the possibility of other gene involved in the pathogenesis.
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Authors
Xiaoling Yang, Ping Qian, Xiaojing Xu, Xiaoyan Liu, Xiru Wu, Yuehua Zhang, Zhixian Yang,