相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。The genetic background of Parkinson's disease: current progress and future prospects
K. Kalinderi et al.
ACTA NEUROLOGICA SCANDINAVICA (2016)
Heterozygote carriers for CNVs in PARK2 are at increased risk of Parkinson's disease
Johanna Huttenlocher et al.
HUMAN MOLECULAR GENETICS (2015)
Analysis of Dosage Mutation in PARK2 among Korean Patients with Early-Onset or Familial Parkinson's Disease
Min Kyung Chu et al.
JOURNAL OF CLINICAL NEUROLOGY (2014)
The Genetics of Parkinson's Disease: Progress and Therapeutic Implications
Andrew B. Singleton et al.
MOVEMENT DISORDERS (2013)
Genetics of Parkinson's disease: the yield
Marianna Spatola et al.
PARKINSONISM & RELATED DISORDERS (2013)
Systematic Review and UK-Based Study of PARK2 (parkin), PINK1, PARK7 (DJ-1) and LRRK2 in early-onset Parkinson's disease
Laura L. Kilarski et al.
MOVEMENT DISORDERS (2012)
Copy Number Variation in Familial Parkinson Disease
Nathan Pankratz et al.
PLOS ONE (2011)
Genetic Etiology of Parkinson Disease Associated with Mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 Genes: A Mutation Update
Karen Nuytemans et al.
HUMAN MUTATION (2010)
Mutation analysis of Parkin, PINK1 and DJ-1 genes in Chinese patients with sporadic early onset parkinsonism
Ji-feng Guo et al.
JOURNAL OF NEUROLOGY (2010)
A comprehensive analysis of deletions, multiplications, and copy number variations in PARK2
D. M. Kay et al.
NEUROLOGY (2010)
Relative Contribution of Simple Mutations vs. Copy Number Variations in Five Parkinson Disease Genes in the Belgian Population
Karen Nuytemans et al.
HUMAN MUTATION (2009)
Parkin and PINK1 mutations in early-onset Parkinson's disease: comprehensive screening in publicly available cases and control
J. Brooks et al.
JOURNAL OF MEDICAL GENETICS (2009)
Parkin dosage mutations have greater pathogenicity in familial PD than simple sequence mutations
N. Pankratz et al.
NEUROLOGY (2009)
Frequency of heterozygous Parkin mutations in healthy subjects: Need for careful prospective follow-up examination of mutation carriers
Norbert Brueggemann et al.
PARKINSONISM & RELATED DISORDERS (2009)
Risk of Parkinson disease in carriers of Parkin mutations - Estimation using the kin-cohort method
Yuanjia Wang et al.
ARCHIVES OF NEUROLOGY (2008)
Rare heterozygous parkin variants in French early-onset Parkinson disease patients and controls
S. Lesage et al.
JOURNAL OF MEDICAL GENETICS (2008)
Deciphering the role of heterozygous mutations in genes associated with parkinsonism
Christine Klein et al.
LANCET NEUROLOGY (2007)
Effective quantitative real-time polymerase chain reaction analysis of the parkin gene (PARK2) exon 1-12 dosage
Maria I. Shadrina et al.
BMC MEDICAL GENETICS (2007)
Heterozygous parkin point mutations are as common in control subjects as in Parkinson's patients
Denise M. Kay et al.
ANNALS OF NEUROLOGY (2007)
A common leucine-rich repeat kinase 2 gene mutation in familial and sporadic Parkinson's disease in Russia
S. N. Illarioshkin et al.
EUROPEAN JOURNAL OF NEUROLOGY (2007)
Influence of heterozygosity for Parkin mutation on onset age in familial Parkinson disease : The GenePD study
Mei Sun et al.
ARCHIVES OF NEUROLOGY (2006)
Case-control study of the Parkin gene in early-onset Parkinson disease
LN Clark et al.
ARCHIVES OF NEUROLOGY (2006)
Parkin mutations and early-onset parkinsonism in a Taiwanese cohort
RM Wu et al.
ARCHIVES OF NEUROLOGY (2005)
Distribution, type, and origin of Parkin mutations:: Review and case studies
K Hedrich et al.
MOVEMENT DISORDERS (2004)
Movement disorder society task force report on the Hoehn and Yahr staging scale: Status and recommendations
CG Goetz et al.
MOVEMENT DISORDERS (2004)
Coding polymorphisms in the parkin gene and susceptibility to Parkinson disease
CB Lücking et al.
ARCHIVES OF NEUROLOGY (2003)
Parkin mutations are frequent in patients with isolated early-onset parkinsonism
M Periquet et al.
BRAIN (2003)
Parkin mutations and susceptibility alleles in late-onset Parkinson's disease
SA Oliveira et al.
ANNALS OF NEUROLOGY (2003)
Parkin variants in north American Parkinson's disease: Cases and controls
SJ Lincoln et al.
MOVEMENT DISORDERS (2003)
Complex relationship between parkin mutations and Parkinson disease
A West et al.
AMERICAN JOURNAL OF MEDICAL GENETICS (2002)
Association between early-onset Parkinson's disease and mutations in the parkin gene
CB Lücking et al.
NEW ENGLAND JOURNAL OF MEDICINE (2000)
Macular microcirculation characteristics in Parkinson's disease evaluated by OCT-Angiography: a literature review
Evita Evangelia Christou et al.
SEMINARS IN OPHTHALMOLOGY