Associated Papers
Uncovering common genetic risk factors in migraine and epilepsy through whole exome sequencing.
Sahu P et al.
Epileptic Disorders : International Epilepsy Journal With Videotape, 2025
Functional Characterization and Pathogenicity Classification of PRRT2 Splice Variants in PRRT2-Related Disorders.
Xu JJ et al.
Annals of Clinical and Translational Neurology, 2025
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