Analysis of PRKN Variants and Clinical Features in Polish Patients with Parkinson’s Disease

The etiology of Parkinson’s disease (PD) is still unclear, but mutations in PRKN have provided some biological insights. The role of PRKN mutations and other genetic variation in determining the clinical features of PD remains unresolved. The aim of the study was to analyze PRKN mutations in PD and...

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Detalles Bibliográficos
Autores principales: Oczkowska, Anna, Florczak-Wyspianska, Jolanta, Permoda-Osip, Agnieszka, Owecki, Michal, Lianeri, Margarita, Kozubski, Wojciech, Dorszewska, Jolanta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Science Publishers 2015
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4765516/
https://www.ncbi.nlm.nih.gov/pubmed/27006626
http://dx.doi.org/10.2174/1389202916666150326002549

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4765516/
https://www.ncbi.nlm.nih.gov/pubmed/27006626
http://dx.doi.org/10.2174/1389202916666150326002549

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