ALG13 participates in epileptogenesis via regulation of GABA(A) receptors in mouse models

ALG13 (asparagine-linked glycosylation 13) plays crucial roles in the process of N-linked glycosylation. Mutations of the ALG13 gene underlie congenital disorders of glycosylation type I (CDG-I), a rare human genetic disorder with defective glycosylation. Epilepsy is commonly observed in congenital...

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Detalles Bibliográficos
Autores principales: Huo, Junming, Ren, Shuanglai, Gao, Peng, Wan, Ding, Rong, Shikuo, Li, Xinxiao, Liu, Shenhai, Xu, Siying, Sun, Kuisheng, Guo, Baorui, Wang, Peng, Yu, Baoli, Wu, Ji, Wang, Feng, Sun, Tao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7499177/
https://www.ncbi.nlm.nih.gov/pubmed/33014431
http://dx.doi.org/10.1038/s41420-020-00319-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7499177/
https://www.ncbi.nlm.nih.gov/pubmed/33014431
http://dx.doi.org/10.1038/s41420-020-00319-6

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