Case of Early-Onset Parkinson’s Disease in a Heterozygous Mutation Carrier of the ATP7B Gene

In this paper, we report a clinically proven case of Parkinson’s disease (PD) with early onset in a patient who is a heterozygous mutation carrier of ATP7B (the Wilson’s disease gene). The patient was observed from 2011 to 2018 in the Center for Neurodegenerative Diseases, Institute of Experimental...

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Detalles Bibliográficos
Autores principales: Ilyechova, Ekaterina Y., Miliukhina, Irina V., Karpenko, Marina N., Orlov, Iurii A., Puchkova, Ludmila V., Samsonov, Sergey A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6789574/
https://www.ncbi.nlm.nih.gov/pubmed/31426520
http://dx.doi.org/10.3390/jpm9030041

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6789574/
https://www.ncbi.nlm.nih.gov/pubmed/31426520
http://dx.doi.org/10.3390/jpm9030041

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