Age-dependent neurological phenotypes in a mouse model of PRRT2-related diseases

Paroxysmal kinesigenic dyskinesia is an episodic movement disorder caused by dominant mutations in the proline-rich transmembrane protein PRRT2, with onset in childhood and typically with improvement or resolution by middle age. Mutations in the same gene may also cause benign infantile seizures, wh...

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Detalles Bibliográficos
Autores principales: AJ, Fay, T, McMahon, C, Im, C, Bair-Marshall, KJ, Niesner, H, Li, A, Nelson, SM, Voglmaier, Y-H, Fu, LJ, Ptáček
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8241743/
https://www.ncbi.nlm.nih.gov/pubmed/34101060
http://dx.doi.org/10.1007/s10048-021-00645-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8241743/
https://www.ncbi.nlm.nih.gov/pubmed/34101060
http://dx.doi.org/10.1007/s10048-021-00645-6

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