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Dissecting the Role of PCDH19 in Clustering Epilepsy by Exploiting Patient-Specific Models of Neurogenesis

PCDH19-related epilepsy is a rare genetic disease caused by defective function of PCDH19, a calcium-dependent cell–cell adhesion protein of the cadherin superfamily. This disorder is characterized by a heterogeneous phenotypic spectrum, with partial and generalized febrile convulsions that are gradu...

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Detalles Bibliográficos
Autores principales:	Borghi, Rossella, Magliocca, Valentina, Petrini, Stefania, Conti, Libenzio Adrian, Moreno, Sandra, Bertini, Enrico, Tartaglia, Marco, Compagnucci, Claudia
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2021
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8268119/ https://www.ncbi.nlm.nih.gov/pubmed/34201522 http://dx.doi.org/10.3390/jcm10132754

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