Cargando…
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...
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: | |
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 |
Ejemplares similares
-
Rare variant in LAMA2 gene causing congenital muscular dystrophy in a Sudanese family. A case report
por: AMIN, MUTAZ, et al.
Publicado: (2019) -
Animal Models of Autosomal Recessive Parkinsonism
por: Bastioli, Guendalina, et al.
Publicado: (2021) -
Good sleep quality is associated with better academic performance among Sudanese medical students
por: Mirghani, Hyder Osman, et al.
Publicado: (2015) -
Frequency of c.35delG Mutation in GJB2 Gene (Connexin 26) in Syrian Patients with Nonsyndromic Hearing Impairment
por: Kaheel, Hazem, et al.
Publicado: (2017) -
Frequency of mitochondrial m.1555A > G mutation in Syrian patients with non-syndromic hearing impairment
por: Kaheel, Hazem, et al.
Publicado: (2018)