about
Association between early-onset Parkinson disease and 22q11.2 deletion syndrome: identification of a novel genetic form of Parkinson disease and its clinical implicationsCopy number variability in Parkinson's disease: assembling the puzzle through a systems biology approachAn evaluation of copy number variation detection tools for cancer using whole exome sequencing data.Copy number deletion has little impact on gene expression levels in racehorses.The emerging role of guanine nucleotide exchange factors in ALS and other neurodegenerative diseases.A PARK2 polymorphism associated with delayed neuropsychological sequelae after carbon monoxide poisoningHigh-resolution survey in familial Parkinson disease genes reveals multiple independent copy number variation events in PARK2Use of the MLPA assay in the molecular diagnosis of gene copy number alterations in human genetic diseases.Copy number polymorphism in plant genomesUsing genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease.Increased Rate of Sporadic and Recurrent Rare Genic Copy Number Variants in Parkinson's Disease Among Ashkenazi JewsNext-generation sequencing in understanding complex neurological diseaseGenome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder.Low-Frequency Copy-Number Variants and General Cognitive Ability: No Evidence of Association.Dock protein family in brain development and neurological disease.Association studies of sporadic Parkinson's disease in the genomic era.Second mutation in PARK2 is absent in patients with sporadic Parkinson's disease and heterozygous exonic deletions/duplications in parkin gene.A customized high-resolution array-comparative genomic hybridization to explore copy number variations in Parkinson's diseaseGStream: improving SNP and CNV coverage on genome-wide association studies.CNVinspector: a web-based tool for the interactive evaluation of copy number variations in single patients and in cohorts.High frequency of Parkin exon rearrangements in Mexican-mestizo patients with early-onset Parkinson's disease.Analysis of chromosomal structural variation in patients with congenital left-sided cardiac lesions.Rare copy number variants in patients with congenital conotruncal heart defects.Heterozygote carriers for CNVs inPARK2are at increased risk of Parkinson's disease
P2860
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P2860
description
2011 nî lūn-bûn
@nan
2011 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Copy number variation in familial Parkinson disease.
@ast
Copy number variation in familial Parkinson disease.
@en
type
label
Copy number variation in familial Parkinson disease.
@ast
Copy number variation in familial Parkinson disease.
@en
prefLabel
Copy number variation in familial Parkinson disease.
@ast
Copy number variation in familial Parkinson disease.
@en
P2093
P2860
P50
P1433
P1476
Copy number variation in familial Parkinson disease.
@en
P2093
Cheryl Halter
Jemma B Wilk
Kimberly F Doheny
Kurt N Hetrick
PSG-PROGENI and GenePD Investigators, Coordinators and Molecular Genetic Laboratories
William C Nichols
P2860
P304
P356
10.1371/JOURNAL.PONE.0020988
P407
P50
P577
2011-08-02T00:00:00Z