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PARK3, Ubiquitin Hydrolase-L1 and Other PD Loci
Rejko Krüger
*
, Olaf Riess
*
Corresponding author for this work
Research output
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Chapter in Book/Report/Conference proceeding
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Chapter
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peer-review
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Citation (Scopus)
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Keyphrases
Parkinson's Disease
100%
Alpha-synuclein (α-syn)
100%
UCHL1
100%
PARK3
100%
Autosomal Recessive Inheritance
66%
Gene Locus
66%
Parkinson Patients
33%
Protein Degradation
33%
PARK2
33%
PARK6
33%
PARK4
33%
PARK7
33%
Gene Products
33%
Parkin
33%
Genetic Heterogeneity
33%
Disease Genes
33%
Early Parkinson's Disease
33%
Genetic Analysis
33%
Genetic Characterization
33%
Large Families
33%
Interacting Proteins
33%
Synphilin-1
33%
Genetic Mapping
33%
Rare mutation
33%
Mapping Approach
33%
Neurofilament
33%
Chromosome 8p
33%
Chromosome 5q
33%
Linkage Analysis
33%
Altered Proteins
33%
Chromosome 17q
33%
Biochemistry, Genetics and Molecular Biology
PARK3
100%
Synuclein
100%
Deubiquitylating Enzyme
100%
Genetics
66%
Gene Locus
66%
Genetic Heterogeneity
33%
Hydrolase
33%
Candidate Gene
33%
Protein Catabolism
33%
PARK7
33%
Gene Product
33%
Linkage Analysis
33%
Chromosome 17q
33%
Autosomal Recessive Inheritance
33%
Ubiquitin C
33%
Chromosome 5q
33%
C-Terminus
33%
Neurofilament
33%
Autosomal Dominant Inheritance
33%
Gene Linkage
33%
Chromosome 8p
33%
Gene Mapping
33%