High frequency of Parkin exon rearrangements in Mexican-mestizo patients with early-onset Parkinson's disease

Analysis of PARK2 gene exon rearrangements in Russian patients with sporadic Parkinson's disease

(2011) Elena V. Semenova et al.   MOVEMENT DISORDERS

Copy Number Variation in Familial Parkinson Disease

(2011) Nathan Pankratz et al.   PLoS One

Mechanisms of Genomic Instabilities Underlying Two Common Fragile-Site-Associated Loci, PARK2 and DMD, in Germ Cell and Cancer Cell Lines

(2010) Jun Mitsui et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Predictors of Parkin Mutations in Early-Onset Parkinson Disease

(2010) Karen S. Marder et al.   ARCHIVES OF NEUROLOGY

Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update

(2010) Karen Nuytemans et al.   HUMAN MUTATION

Parkin Directly Modulates 26S Proteasome Activity

(2010) J. W. Um et al.   JOURNAL OF NEUROSCIENCE

A comprehensive analysis of deletions, multiplications, and copy number variations in PARK2

(2010) D. M. Kay et al.   NEUROLOGY

Parkinson's disease: from monogenic forms to genetic susceptibility factors

(2009) S. Lesage et al.   HUMAN MOLECULAR GENETICS

Genetic screening reveals high frequency of PARK2 mutations and reduced Parkin expression conferring risk for Parkinsonism in North West India

(2009) M. Vinish et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

Bacterial Artificial Chromosome Transgenic Mice Expressing a Truncated Mutant Parkin Exhibit Age-Dependent Hypokinetic Motor Deficits, Dopaminergic Neuron Degeneration, and Accumulation of Proteinase K-Resistant  -Synuclein

(2009) X.-H. Lu et al.   JOURNAL OF NEUROSCIENCE

Analysis of exon dosage using MLPA in South African Parkinson's disease patients

(2009) Rowena J. Keyser et al.   NEUROGENETICS

Parkin dosage mutations have greater pathogenicity in familial PD than simple sequence mutations

(2009) N. Pankratz et al.   NEUROLOGY

Frequency of heterozygous Parkin mutations in healthy subjects: Need for careful prospective follow-up examination of mutation carriers

(2009) Norbert Brüggemann et al.   PARKINSONISM & RELATED DISORDERS

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

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