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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Pubblicato in:Adv Bioinformatics
Autori principali: Bakhit, Yousuf Hasan Yousuf, Ibrahim, Mohamed Osama Mirghani, Amin, Mutaz, Mirghani, Yousra Abdelazim, Hassan, Mohamed Ahmed Salih
Natura: Artigo
Lingua:Inglês
Pubblicazione: Hindawi Publishing Corporation 2016
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Research Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC5227114/
https://ncbi.nlm.nih.gov/pubmed/28127307
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2016/9313746
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