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Genomic instability in the PARK2 locus is associated with Parkinson’s disease

Parkinson’s disease (PD) is a common neurodegenerative disorder affecting mostly elderly people, although there is a group of patients developing so-called early-onset PD (EOPD). Mutations in the PARK2 gene are a common cause of autosomal recessive EOPD. PARK2 belongs to the family of extremely larg...

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Detalhes bibliográficos
Publicado no:J Appl Genet
Main Authors: Ambroziak, Wojciech, Koziorowski, Dariusz, Duszyc, Kinga, Górka-Skoczylas, Paulina, Potulska-Chromik, Anna, Sławek, Jarosław, Hoffman-Zacharska, Dorota
Formato: Artigo
Idioma:Inglês
Publicado em: Springer Berlin Heidelberg 2015
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4617850/
https://ncbi.nlm.nih.gov/pubmed/25833766
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s13353-015-0282-9
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