PRRT2 Mutant Leads to Dysfunction of Glutamate Signaling

Paroxysmal kinesigenic choreoathetosis (PKC) is an inherited disease of the nervous system. We previously identified PRRT2 as the causative gene of PKC. However, as little is known about the function of PRRT2, elucidating its function will benefit not only PKC studies, but also many other related di...

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Detalles Bibliográficos
Autores principales: Li, Ming, Niu, Fenghe, Zhu, Xilin, Wu, Xiaopan, Shen, Ning, Peng, Xiaozhong, Liu, Ying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4463582/
https://www.ncbi.nlm.nih.gov/pubmed/25915028
http://dx.doi.org/10.3390/ijms16059134

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4463582/
https://www.ncbi.nlm.nih.gov/pubmed/25915028
http://dx.doi.org/10.3390/ijms16059134

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