Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations: evidence for oligogenic inheritance.
about
Whole-genome sequencing suggests mechanisms for 22q11.2 deletion-associated Parkinson's disease.Mechanisms of Gene-Environment Interactions in Parkinson's Disease.New Genes Causing Hereditary Parkinson's Disease or Parkinsonism.The role of gene variants in the pathogenesis of neurodegenerative disorders as revealed by next generation sequencing studies: a review.Taking out the garbage: cathepsin D and calcineurin in neurodegeneration.Excessive burden of lysosomal storage disorder gene variants in Parkinson's disease.OligoPVP: Phenotype-driven analysis of individual genomic information to prioritize oligogenic disease variants
P2860
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P2860
Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations: evidence for oligogenic inheritance.
description
2016 nî lūn-bûn
@nan
2016 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2016 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
name
Additional rare variant analys ...... ce for oligogenic inheritance.
@ast
Additional rare variant analys ...... ce for oligogenic inheritance.
@en
type
label
Additional rare variant analys ...... ce for oligogenic inheritance.
@ast
Additional rare variant analys ...... ce for oligogenic inheritance.
@en
prefLabel
Additional rare variant analys ...... ce for oligogenic inheritance.
@ast
Additional rare variant analys ...... ce for oligogenic inheritance.
@en
P2093
P2860
P50
P356
P1476
Additional rare variant analys ...... ce for oligogenic inheritance.
@en
P2093
Adam P Levine
Alan M Pittman
Alastair J Noyce
Aude Nicolas
Elena R Schiff
Huw R Morris
Iris E Jansen
J Raphael Gibbs
James E Tomkins
P2860
P304
P356
10.1093/HMG/DDW348
P50
P577
2016-10-18T00:00:00Z