YWHAG Mutations Cause Childhood Myoclonic Epilepsy and Febrile Seizures: Molecular Sub-regional Effect and Mechanism

YWHAG, which encodes an adapter protein 14-3-3γ, is highly expressed in the brain and regulates a diverse range of cell signaling pathways. Previously, eight YWHAG mutations have been identified in patients with epileptic encephalopathy (EE). In this study, using trios-based whole exome sequencing,...

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Detalles Bibliográficos
Autores principales: Ye, Xing-Guang, Liu, Zhi-Gang, Wang, Jie, Dai, Jie-Min, Qiao, Pei-Xiu, Gao, Ping-Ming, Liao, Wei-Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7985244/
https://www.ncbi.nlm.nih.gov/pubmed/33767733
http://dx.doi.org/10.3389/fgene.2021.632466

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7985244/
https://www.ncbi.nlm.nih.gov/pubmed/33767733
http://dx.doi.org/10.3389/fgene.2021.632466

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