Analysis of Dosage Mutation in PARK2 among Korean Patients with Early-Onset or Familial Parkinson's Disease
about
Copy number variability in Parkinson's disease: assembling the puzzle through a systems biology approachDysregulation of the causative genes for hereditary parkinsonism in the midbrain in Parkinson's disease.Second mutation in PARK2 is absent in patients with sporadic Parkinson's disease and heterozygous exonic deletions/duplications in parkin gene.The M458L missense mutation disrupts the catalytic properties of Parkin.
P2860
Analysis of Dosage Mutation in PARK2 among Korean Patients with Early-Onset or Familial Parkinson's Disease
description
2014 nî lūn-bûn
@nan
2014 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի հուլիսին հրատարակված գիտական հոդված
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2014年の論文
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2014年論文
@yue
2014年論文
@zh-hant
2014年論文
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2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
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name
Analysis of Dosage Mutation in ...... r Familial Parkinson's Disease
@ast
Analysis of Dosage Mutation in ...... r Familial Parkinson's Disease
@en
type
label
Analysis of Dosage Mutation in ...... r Familial Parkinson's Disease
@ast
Analysis of Dosage Mutation in ...... r Familial Parkinson's Disease
@en
prefLabel
Analysis of Dosage Mutation in ...... r Familial Parkinson's Disease
@ast
Analysis of Dosage Mutation in ...... r Familial Parkinson's Disease
@en
P2093
P2860
P1476
Analysis of Dosage Mutation in ...... r Familial Parkinson's Disease
@en
P2093
Hyeo-Il Ma
Jeong-Hoon Hong
Jung Mi Choi
Min Kyung Chu
Suk Yun Kang
Won Chan Kim
Yun Joong Kim
P2860
P304
P356
10.3988/JCN.2014.10.3.244
P577
2014-07-03T00:00:00Z