PCDH19-Related Epilepsy Syndrome: A Comprehensive Clinical Review
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology,Developmental Neuroscience,Neurology,Pediatrics, Perinatology, and Child Health
Reference41 articles.
1. A new familial form of convulsivedisorder and mental retardation limited to females;Juberg;J Pediatr,1971
2. Epilepsy and mental retardation limited to females: an X-linked dominant disorder with male sparing;Ryan;Nat Genet,1997
3. X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment;Dibbens;Nat Genet,2008
4. Structural determinants of adhesion by Protocadherin-19 and implications for its role in epilepsy;Cooper;Elife,2016
5. The role of protocadherin 19 (PCDH19) in neurodevelopment and in the pathophysiology of early infantile epileptic encephalopathy-9 (EIEE9);Gerosa;Dev Neurobiol,2019
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