DOI:
10.1055/s-00029030
Journal of Pediatric Neurology
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References
Lilles S, Talvik I, Noormets K. et al.
CDKL5 gene-related epileptic encephalopathy in estonia: four cases, one novel mutation causing severe phenotype in a boy, and overview of the literature.
Neuropediatrics 2016;
47 (06) 361-367
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