High-resolution survey in familial Parkinson disease genes reveals multiple independent copy number variation events in PARK2
about
Copy number variability in Parkinson's disease: assembling the puzzle through a systems biology approachCopy number gain of VCX, X-linked multi-copy gene, leads to cell proliferation and apoptosis during spermatogenesis.Single-nucleotide polymorphisms and haplotypes of non-coding area in the CP gene are correlated with Parkinson's diseaseHigh-resolution arrays reveal burden of copy number variations on Parkinson disease genes associated with increased disease risk in random cohorts.A customized high-resolution array-comparative genomic hybridization to explore copy number variations in Parkinson's diseaseHeterozygote carriers for CNVs inPARK2are at increased risk of Parkinson's disease
P2860
High-resolution survey in familial Parkinson disease genes reveals multiple independent copy number variation events in PARK2
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
2013年论文
@zh
2013年论文
@zh-cn
name
High-resolution survey in fami ...... mber variation events in PARK2
@ast
High-resolution survey in fami ...... mber variation events in PARK2
@en
type
label
High-resolution survey in fami ...... mber variation events in PARK2
@ast
High-resolution survey in fami ...... mber variation events in PARK2
@en
prefLabel
High-resolution survey in fami ...... mber variation events in PARK2
@ast
High-resolution survey in fami ...... mber variation events in PARK2
@en
P2093
P2860
P50
P356
P1433
P1476
High-resolution survey in fami ...... mber variation events in PARK2
@en
P2093
Cherylyn Jauregui
Eden R Martin
Karen Nuytemans
Liyong Wang
William K Scott
P2860
P304
P356
10.1002/HUMU.22344
P577
2013-05-28T00:00:00Z