CDKL5 Gene-Related Epileptic Encephalopathy in Estonia: Four Cases, One Novel Mutation Causing Severe Phenotype in a Boy, and Overview of the Literature

Title
CDKL5 Gene-Related Epileptic Encephalopathy in Estonia: Four Cases, One Novel Mutation Causing Severe Phenotype in a Boy, and Overview of the Literature
Authors
Keywords
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Journal
NEUROPEDIATRICS
Volume 47, Issue 06, Pages 361-367
Publisher
Georg Thieme Verlag KG
Online
2016-09-07
DOI
10.1055/s-0036-1586730

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