Clinical Manifestations in Paroxysmal Kinesigenic Dyskinesia Patients with Proline-Rich Transmembrane Protein 2 Gene Mutation

BACKGROUND AND PURPOSE: Given the diverse phenotypes including combined non-dyskinetic symptoms in patients harboring mutations of the gene encoding proline-rich transmembrane protein 2 (PRRT2), the clinical significance of these mutations in paroxysmal kinesigenic dyskinesia (PKD) is questionable....

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Detalles Bibliográficos
Autores principales: Youn, Jinyoung, Kim, Ji Sun, Lee, Munhyang, Lee, Jeehun, Roh, Hakjae, Ki, Chang-Seok, Choa, Jin Whan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Neurological Association 2014
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3896649/
https://www.ncbi.nlm.nih.gov/pubmed/24465263
http://dx.doi.org/10.3988/jcn.2014.10.1.50

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3896649/
https://www.ncbi.nlm.nih.gov/pubmed/24465263
http://dx.doi.org/10.3988/jcn.2014.10.1.50

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