Novel CSNK2B Mutation Sheds Light on Epilepsy Severity in Rare Syndrome
A newly identified CSNK2B mutation in a Chinese family with early-onset seizures joins an analysis of 103 cases suggesting protein-level ...
Tag: seizure onset
A newly identified CSNK2B mutation in a Chinese family with early-onset seizures joins an analysis of 103 cases suggesting protein-level ...
