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Publications by Christine Klein
CLPB Mutations Cause 3-Methylglutaconic Aciduria, Progressive Brain Atrophy, Intellectual Disability, Congenital Neutropenia, Cataracts, Movement Disorder
American Journal of Human Genetics
Genetics
MtDNA Deletions Discriminate Affected From Unaffected LRRK2 Mutation Carriers
Annals of Neurology
Neurology
Association of Pallidal Neurostimulation and Outcome Predictors With X-Linked Dystonia Parkinsonism
JAMA Neurology
Neurology
Risky Behaviors and Parkinson Disease
Neurology
Neurology
Phenomenology and Classification of Dystonia: A Consensus Update
Movement Disorders
Neurology
Mild Dopa-Responsive Dystonia in Heterozygous Tyrosine Hydroxylase Mutation Carrier: Evidence of Symptomatic Enzyme Deficiency?
Parkinsonism and Related Disorders
Gerontology
Geriatrics
Neurology
The Role of Rare Coding Variants in Parkinson's Disease GWAS Loci
Frontiers in Neurology
Neurology
Profiling of Parkin-Binding Partners Using Tandem Affinity Purification
PLoS ONE
Multidisciplinary
First Report of a Filipino With Mohr-Tranebjaerg Syndrome
Movement Disorders Clinical Practice
Neurology
Importance of Tissue Selection for Genetic Testing: Detection of a Terminal 18q Deletion After Stem Cell Transplantation
Movement Disorders Clinical Practice
Neurology
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