A somatic mutation in MEN1 gene detected in periventricular nodular heterotopia tissue obtained from depth electrodes

Periventricular nodular heterotopia (PNH) is a common structural malformation of cortical development. Mutations in the filamin A gene are frequent in familial cases with X‐linked PNH. However, many cases with sporadic PNH remain genetically unexplained. Although medically refractory epilepsy often...

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Detalles Bibliográficos
Autores principales: Montier, Laura, Haneef, Zulfi, Gavvala, Jay, Yoshor, Daniel, North, Robert, Verla, Terence, Van Ness, Paul C., Drabek, Janice, Goldman, Alica M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Brief Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6852559/
https://www.ncbi.nlm.nih.gov/pubmed/31489630
http://dx.doi.org/10.1111/epi.16328

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6852559/
https://www.ncbi.nlm.nih.gov/pubmed/31489630
http://dx.doi.org/10.1111/epi.16328

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