Associated Papers
Landau-Kleffner Syndrome Can Herald the Diagnosis of GRIN2A Gene Mutation.
Ebrahim AK et al.
Case Reports in Pediatrics, 2025
Clinical phenotype and functional influence of GRIN2A variants in epilepsy-aphasia syndrome.
Zhang L et al.
Epilepsia Open, 2024
39474911 (PubMed )
Supplement: EPI4-9-2306-s002.xlsx › Sheet1
GRIN2A Variants Associated With Idiopathic Generalized Epilepsies.
Liu XR et al.
Frontiers in Molecular Neuroscience, 2021
34720871 (PubMed )
Supplement: Table_3.docx
[Study of GRIN2A mutation in epilepsy-aphasia spectrum disorders].
Qian P et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics, 2018
GRIN2A mutations in epilepsy-aphasia spectrum disorders.
Yang X et al.
Brain & Development, 2018
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