Implication of sestrin3 in epilepsy and its comorbidities

Epilepsy is a serious neurological disorder affecting about 1% of the population worldwide. Epilepsy may arise as a result of acquired brain injury, or as a consequence of genetic predisposition. To date, genome-wide association studies and exome sequencing approaches have provided limited insights...

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Detalles Bibliográficos
Autores principales: Lovisari, Francesca, Roncon, Paolo, Soukoupova, Marie, Paolone, Giovanna, Labasque, Marilyne, Ingusci, Selene, Falcicchia, Chiara, Marino, Pietro, Johnson, Michael, Rossetti, Tiziana, Petretto, Enrico, Leclercq, Karine, Kaminski, Rafal M, Moyon, Ben, Webster, Zoe, Simonato, Michele, Zucchini, Silvia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7966953/
https://www.ncbi.nlm.nih.gov/pubmed/33758823
http://dx.doi.org/10.1093/braincomms/fcaa130

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7966953/
https://www.ncbi.nlm.nih.gov/pubmed/33758823
http://dx.doi.org/10.1093/braincomms/fcaa130

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