Relative contribution of simple mutations vs. copy number variations in five Parkinson disease genes in the Belgian population. - Wikidata - awgldk - TriplyDB

Relative contribution of simple mutations vs. copy number variations in five Parkinson disease genes in the Belgian population.

Relative contribution of simple mutations vs. copy number variations in five Parkinson disease genes in the Belgian population.

http://www.wikidata.org/entity/Q47910797

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Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update Copy number variability in Parkinson's disease: assembling the puzzle through a systems biology approach Increasing the Coding Potential of Genomes Through Alternative Splicing: The Case of PARK2 Gene.Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study.Genome wide association studies and prion disease.High-resolution survey in familial Parkinson disease genes reveals multiple independent copy number variation events in PARK2 Predictors of parkin mutations in early-onset Parkinson disease: the consortium on risk for early-onset Parkinson disease study.Splicing: is there an alternative contribution to Parkinson's disease?α-Synucleinopathy associated with G51D SNCA mutation: a link between Parkinson's disease and multiple system atrophy?Genetic analysis of PARK2 and PINK1 genes in Brazilian patients with early-onset Parkinson's disease Genetic insights into sporadic Parkinson's disease pathogenesis.LRRK2: cause, risk, and mechanism.Recent advances in α-synuclein functions, advanced glycation, and toxicity: implications for Parkinson's disease.Impulse control disorders in Parkinson's disease: an overview from neurobiology to treatment.Second mutation in PARK2 is absent in patients with sporadic Parkinson's disease and heterozygous exonic deletions/duplications in parkin gene.Deep sequencing of the LRRK2 gene in 14,002 individuals reveals evidence of purifying selection and independent origin of the p.Arg1628Pro mutation in Europe.Guanosine triphosphate cyclohydrolase 1 promoter deletion causes dopa-responsive dystonia.Genetic analysis of SNCA coding mutation in Chinese Han patients with Parkinson disease.Novel compound heterozygous mutations in the PARK2 gene identified in a Chinese pedigree with early-onset Parkinson's disease.Heterozygote carriers for CNVs inPARK2are at increased risk of Parkinson's disease

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P2860

Relative contribution of simple mutations vs. copy number variations in five Parkinson disease genes in the Belgian population.

http://www.wikidata.org/entity/Q47910797

description

2009 nî lūn-bûn

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2009年の論文

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2009年学术文章

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2009年学术文章

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2009年学术文章

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2009年学术文章

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2009年学术文章

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2009年学术文章

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2009年學術文章

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Relative contribution of simpl ...... nes in the Belgian population.

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Relative contribution of simpl ...... nes in the Belgian population.

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Relative contribution of simpl ...... nes in the Belgian population.

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Relative contribution of simpl ...... nes in the Belgian population.

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Relative contribution of simpl ...... nes in the Belgian population.

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Relative contribution of simpl ...... nes in the Belgian population.

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Relative contribution of simpl ...... nes in the Belgian population.

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Barbara Pickut

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Bram Meeus

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David Crosiers

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Ellen Corsmit

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Jurgen Del-Favero

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Karen Nuytemans

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Marleen Van den Broeck

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Patrick Cras

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Peter P De Deyn

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Philippe Pals

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P2860

Parkinsonism: onset, progression and mortality

DJ-1 (PARK7) mutations are less frequent than Parkin (PARK2) mutations in early-onset Parkinson disease.

A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease

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1054-1061

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10.1002/HUMU.21007

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7

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30

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Christine Van Broeckhoven

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24379859

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19405094

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Parkinson's disease