Genetic Analysis of RAB39B in an Early-Onset Parkinson's Disease Cohort
Published 2020 View Full Article
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Title
Genetic Analysis of RAB39B in an Early-Onset Parkinson's Disease Cohort
Authors
Keywords
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Journal
Frontiers in Neurology
Volume 11, Issue -, Pages -
Publisher
Frontiers Media SA
Online
2020-06-26
DOI
10.3389/fneur.2020.00523
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Related references
Note: Only part of the references are listed.- Clinical and Neuropathological Features Associated With Loss of RAB39B
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- Lack of RAB39B mutations in early-onset and familial Parkinson's disease in a Taiwanese cohort
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- RAB39B gene mutations are not a common cause of Parkinson's disease or dementia with Lewy bodies
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- RAB39B mutations are a rare finding in Parkinson disease patients
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- RAB39B gene mutations are not linked to familial Parkinson’s disease in China
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- (2015) Sue Richards et al. GENETICS IN MEDICINE
- The RAB39B p.G192R mutation causes X-linked dominant Parkinson’s disease
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- High frequency of beta-propeller protein-associated neurodegeneration (BPAN) among patients with intellectual disability and young-onset parkinsonism
- (2015) Kenya Nishioka et al. NEUROBIOLOGY OF AGING
- Mutations in RAB39B Cause X-Linked Intellectual Disability and Early-Onset Parkinson Disease with α-Synuclein Pathology
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- Xq28 duplication overlapping theint22h-1/int22h-2region and includingRAB39BandCLIC2in a family with intellectual and developmental disability
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- DANN: a deep learning approach for annotating the pathogenicity of genetic variants
- (2014) Daniel Quang et al. BIOINFORMATICS
- Increased Dosage of RAB39B Affects Neuronal Development and Could Explain the Cognitive Impairment in Male Patients with Distal Xq28 Copy Number Gains
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- Screening of two indel polymorphisms in the 5′UTR of the DJ-1 gene in South African Parkinson’s disease patients
- (2013) Brigitte Glanzmann et al. JOURNAL OF NEURAL TRANSMISSION
- Mutational Screening of PARKIN Identified a 3′ UTR Variant (rs62637702) Associated with Parkinson’s Disease
- (2012) Lorena de Mena et al. JOURNAL OF MOLECULAR NEUROSCIENCE
- A Search for SNCA 3′ UTR Variants Identified SNP rs356165 as a Determinant of Disease Risk and Onset Age in Parkinson’s Disease
- (2011) Lucía F. Cardo et al. JOURNAL OF MOLECULAR NEUROSCIENCE
- Variation in the miRNA-433 Binding Site of FGF20 Confers Risk for Parkinson Disease by Overexpression of α-Synuclein
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