In Silico Analysis of SNPs in PARK2 and PINK1 Genes That Potentially Cause Autosomal Recessive Parkinson Disease

Introduction. Parkinson's disease (PD) is a common neurodegenerative disorder. Mutations in PINK1 are the second most common agents causing autosomal recessive, early onset PD. We aimed to identify the pathogenic SNPs in PARK2 and PINK1 using in silico prediction software and their effect on th...

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Detalles Bibliográficos
Autores principales: Bakhit, Yousuf Hasan Yousuf, Ibrahim, Mohamed Osama Mirghani, Amin, Mutaz, Mirghani, Yousra Abdelazim, Hassan, Mohamed Ahmed Salih
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5227114/
https://www.ncbi.nlm.nih.gov/pubmed/28127307
http://dx.doi.org/10.1155/2016/9313746

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5227114/
https://www.ncbi.nlm.nih.gov/pubmed/28127307
http://dx.doi.org/10.1155/2016/9313746

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