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。Worldwide frequency of G2019S LRRK2 mutation in Parkinson's disease: A systematic review
L. Correia Guedes et al.
PARKINSONISM & RELATED DISORDERS (2010)
Molecular pathogenesis of Parkinson disease: insights from genetic studies
Thomas Gasser
EXPERT REVIEWS IN MOLECULAR MEDICINE (2009)
LRRK2 Gene Variation and Its Contribution to Parkinson Disease
Coro Paisan-Ruiz
HUMAN MUTATION (2009)
A Clinic-Based Screening of Mutations in Exons 31, 34, 35, 41, and 48 of LRRK2 in Iranian Parkinson's Disease Patients
Seyedmehdi Shojaee et al.
MOVEMENT DISORDERS (2009)
Genetic analysis for five LRRK2 mutations in a Sardinian parkinsonian population: Importance of G2019S and R1441C mutations in sporadic Parkinson's disease patients
Gianluca Floris et al.
PARKINSONISM & RELATED DISORDERS (2009)
Genetic screening for LRRK2 gene G2019S mutation in Parkinson's disease patients from Southern Italy
Anna De Rosa et al.
PARKINSONISM & RELATED DISORDERS (2009)
Founder mutation p.R1441C in the leucine-rich repeat kinase 2 gene in Belgian Parkinson's disease patients
Karen Nuytemans et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2008)
Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study
Daniel G. Healy et al.
LANCET NEUROLOGY (2008)
Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease
K. Haugarvoll et al.
NEUROLOGY (2008)
Global distribution and reduced penetrance: Lrrk2 R1441C in an Irish Parkinson's disease kindred
David Gosal et al.
MOVEMENT DISORDERS (2007)
Analysis of 14 LRRK2 mutations in Parkinson's plus syndromes and late-onset Parkinson's disease
E. K. Tan et al.
MOVEMENT DISORDERS (2006)
Comprehensive analysis of the LRRK2 gene in sixty families with Parkinson's disease
A Di Fonzo et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2006)
The G6055A (G2019S) mutation in LRRK2 is frequent in both early and late onset Parkinson's disease and originates from a common ancestor -: art. no. e65
S Goldwurm et al.
JOURNAL OF MEDICAL GENETICS (2005)
Mutations in LRRK2 cause autosomal-dominant Parkinsonism with pleomorphic pathology
A Zimprich et al.
NEURON (2004)
Macular microcirculation characteristics in Parkinson's disease evaluated by OCT-Angiography: a literature review
Evita Evangelia Christou et al.
SEMINARS IN OPHTHALMOLOGY