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

Internet

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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