Modifying PCDH19 levels affects cortical interneuron migration

PCDH19 is a transmembrane protein and member of the protocadherin family. It is encoded by the X-chromosome and more than 200 mutations have been linked to the neurodevelopmental PCDH-clustering epilepsy (PCDH19-CE) syndrome. A disturbed cell-cell contact that arises when random X-inactivation creat...

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Detalles Bibliográficos
Autores principales: Pancho, Anna, Mitsogiannis, Manuela D., Aerts, Tania, Dalla Vecchia, Marco, Ebert, Lena K., Geenen, Lieve, Noterdaeme, Lut, Vanlaer, Ria, Stulens, Anne, Hulpiau, Paco, Staes, Katrien, Van Roy, Frans, Dedecker, Peter, Schermer, Bernhard, Seuntjens, Eve
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9642031/
https://www.ncbi.nlm.nih.gov/pubmed/36389226
http://dx.doi.org/10.3389/fnins.2022.887478

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9642031/
https://www.ncbi.nlm.nih.gov/pubmed/36389226
http://dx.doi.org/10.3389/fnins.2022.887478

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