Genetic analysis of SNCA coding mutation in Chinese Han patients with Parkinson disease

Genetic variants and animal models in SNCA and Parkinson disease

(2014) Hao Deng et al.   AGEING RESEARCH REVIEWS

G51D α-synuclein mutation causes a novel Parkinsonian-pyramidal syndrome

(2013) Suzanne Lesage et al.   ANNALS OF NEUROLOGY

Mutation in theSYNJ1Gene Associated with Autosomal Recessive, Early-Onset Parkinsonism

(2013) Marialuisa Quadri et al.   HUMAN MUTATION

Somatic alpha-synuclein mutations in Parkinson's disease: Hypothesis and preliminary data

(2013) Christos Proukakis et al.   MOVEMENT DISORDERS

Alpha-synuclein p.H50Q, a novel pathogenic mutation for Parkinson's disease

(2013) Silke Appel-Cresswell et al.   MOVEMENT DISORDERS

A novel  -synuclein missense mutation in Parkinson disease

(2013) C. Proukakis et al.   NEUROLOGY

Genetic analysis of the FBXO48 gene in Chinese Han patients with Parkinson disease

(2013) Xiaofei Xiu et al.   NEUROSCIENCE LETTERS

EIF4G1 Ala502Val and Arg1205His variants in Chinese patients with Parkinson disease

(2013) Lamei Yuan et al.   NEUROSCIENCE LETTERS

Genetic analysis of the S100B gene in Chinese patients with Parkinson disease

(2013) Yi Guo et al.   NEUROSCIENCE LETTERS

Monogenic Parkinson's disease and parkinsonism: Clinical phenotypes and frequencies of known mutations

(2013) Andreas Puschmann   PARKINSONISM & RELATED DISORDERS

F-Box Only Protein 7 Gene in Parkinsonian-Pyramidal Disease

(2013) Hao Deng et al.   JAMA Neurology

VPS35mutation in Chinese Han patients with late-onset Parkinson's disease

(2012) H. Deng et al.   EUROPEAN JOURNAL OF NEUROLOGY

Analysis of LRRK2, SNCA, Parkin, PINK1, and DJ-1 in Zambian patients with Parkinson's disease

(2012) Ekaterina Yonova-Doing et al.   PARKINSONISM & RELATED DISORDERS

Extensive enteric nervous system abnormalities in mice transgenic for artificial chromosomes containing Parkinson disease-associated α-synuclein gene mutations precede central nervous system changes

(2010) Yien-Ming Kuo et al.   HUMAN MOLECULAR GENETICS

Relative contribution of simple mutations vs. copy number variations in five Parkinson disease genes in the Belgian population

(2009) Karen Nuytemans et al.   HUMAN MUTATION

Familial Parkinsonism and early onset Parkinson's disease in a Brazilian movement disorders clinic: Phenotypic characterization and frequency ofSNCA,PRKN,PINK1, andLRRK2mutations

(2009) Sarah Teixeira Camargos et al.   MOVEMENT DISORDERS

Analysis of Parkinson disease patients from Portugal for mutations in SNCA, PRKN, PINK1 and LRRK2

(2008) Jose Bras et al.   BMC Neurology

Parkinson's disease: clinical features and diagnosis

(2008) J Jankovic   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

Screening PARK genes for mutations in early-onset Parkinson's disease patients from Queensland, Australia

(2008) George D. Mellick et al.   PARKINSONISM & RELATED DISORDERS