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Title
TheEIF4G1gene and Parkinson's disease
Authors
Keywords
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Journal
ACTA NEUROLOGICA SCANDINAVICA
Volume 132, Issue 2, Pages 73-78
Publisher
Wiley
Online
2015-03-13
DOI
10.1111/ane.12397
References
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Related references
Note: Only part of the references are listed.- Frequency of the ASP620ASN mutation in VPS35 and Arg1205His mutation in EIF4G1 in familial Parkinson's disease from South Italy
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- Human Eukaryotic Initiation Factor 4G (eIF4G) Protein Binds to eIF3c, -d, and -e to Promote mRNA Recruitment to the Ribosome
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- EIF4G1 R1205H and VPS35 D620N mutations are rare in Parkinson's disease from South Africa
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- Whole exome sequencing of rare variants in EIF4G1 and VPS35 in Parkinson disease
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- EIF4G1 Ala502Val and Arg1205His variants in Chinese patients with Parkinson disease
- (2013) Lamei Yuan et al. NEUROSCIENCE LETTERS
- eIF4GI Facilitates the MicroRNA-Mediated Gene Silencing
- (2013) Incheol Ryu et al. PLoS One
- F-Box Only Protein 7 Gene in Parkinsonian-Pyramidal Disease
- (2013) Hao Deng et al. JAMA Neurology
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- Identifying Consensus Disease Pathways in Parkinson's Disease Using an Integrative Systems Biology Approach
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- Parkinson's disease: clinical features and diagnosis
- (2008) J Jankovic JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
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