Associated Papers
The clinical spectrum associated with ATP1A2 variants in Chinese pediatric patients.
Dai L et al.
Brain & Development, 2023
Epilepsy in hemiplegic migraine: Genetic mutations and clinical implications.
Prontera P et al.
Cephalalgia : an International Journal of Headache, 2018
ExACtly zero or once: A clinically helpful guide to assessing genetic variants in mild epilepsies.
Bennett CA et al.
Neurology. Genetics, 2017
28717674 (PubMed )
Supplement: supp_3.4.e163_Table_e-1.xlsx › Other_neurological_disorders
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