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The Lancet Neurology, ISSN 1474-4422, 12/2018, Volume 17, Issue 12, pp. 1035 - 1036
[...]highly penetrant variants that cause autosomal dominant diseases are usually not observed among individuals with sporadic disease. [...]we argue that the... 
Proteins | Lipoproteins | Brain research | Parkinsons disease | Receptor density | Patients | Data bases | Age | Brain diseases | Dementia
Journal Article
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 03/2012, Volume 90, Issue 3, pp. 467 - 477
Manganese is essential for several metabolic pathways but becomes toxic in excessive amounts. Manganese levels in the body are therefore tightly regulated, but... 
TRANSPORTER | MANGANESE | CIRRHOSIS | GENES | GENETICS & HEREDITY | IDENTIFICATION | ZNT-1 | EXPRESSION | ZINC | FAMILY | Manganese Poisoning - genetics | Zinc Transporter 8 | Humans | Middle Aged | Molecular Sequence Data | Male | Brain - metabolism | Cation Transport Proteins - metabolism | Membrane Transport Proteins - genetics | Chromosome Mapping - methods | Cation Transport Proteins - genetics | Female | Membrane Transport Proteins - metabolism | Parkinsonian Disorders - genetics | Tumor Cells, Cultured | Frameshift Mutation - genetics | Amino Acid Sequence | Genetic Predisposition to Disease | Liver - metabolism | Genes, Recessive | Hep G2 Cells | Immunohistochemistry - methods | Homozygote | Sequence Alignment - methods | Phenotype | Manganese - metabolism | Metabolic Diseases - metabolism | Metabolic Diseases - genetics | Aged | Manganese Poisoning - metabolism | Parkinsonism | Liver diseases | Gene mutations | Causes of | Genetic aspects | Dystonia | Research | Manganese compounds | Physiology | Mutation | Genomics | Neurological disorders | Index Medicus | Brain | Basal ganglia | Central nervous system diseases | Frameshift mutation | Nervous system | Cytosol | Fatty liver | Polycythemia | Substrate specificity | Chelation | Cations | Metabolic pathways | Gene mapping | steatosis | Movement disorders | Manganese
Journal Article
Journal Article
Journal Article
Science, ISSN 0036-8075, 1/2003, Volume 299, Issue 5604, pp. 256 - 259
Journal Article
Annals of Neurology, ISSN 0364-5134, 02/2016, Volume 79, Issue 2, pp. 244 - 256
Journal Article
The Lancet Neurology, ISSN 1474-4422, 07/2018, Volume 17, Issue 7, pp. 597 - 608
Most patients with Parkinson's disease, Parkinson's disease dementia, and dementia with Lewy bodies do not carry mutations in known disease-causing genes. The... 
DIAGNOSIS | MULTICENTER | MANAGEMENT | VPS35 | GLUCOCEREBROSIDASE MUTATIONS | ASSOCIATION | CLINICAL NEUROLOGY | FEATURES | REVEALS | Parkinson Disease - complications | Genome-Wide Association Study | Humans | Middle Aged | RNA, Messenger - genetics | Male | Dementia - epidemiology | Parkinson Disease - genetics | Dementia - genetics | LDL-Receptor Related Proteins - genetics | Lewy Body Disease - epidemiology | Pluripotent Stem Cells - metabolism | Dementia - etiology | Lewy Body Disease - genetics | Pedigree | Brain - pathology | Parkinson Disease - epidemiology | Family | Female | Heterozygote | Italy | RNA, Messenger - chemistry | Chromosomes, Human, Pair 14 - genetics | Genetic Linkage | Genetic research | Genetic aspects | Analysis | Genomics | Dementia | Parkinson's disease | Laboratories | Neuropathology | Immunocytochemistry | Genes | Parkinsons disease | Aneurysm | Genomes | Proteins | Neurodegeneration | Autopsy | Dementia disorders | Aorta | Chromosome 14 | Movement disorders | Deoxyribonucleic acid--DNA | Linkage analysis | Neurodegenerative diseases | Therapeutic applications | Gene expression | Lewy bodies | Genetic variance | Pathology | Cycloheximide | Brain research | Molecular modelling | Pluripotency | mRNA stability | Index Medicus | Neurologi | Clinical Medicine | Neurology | Medical and Health Sciences | Klinisk medicin | Medicin och hälsovetenskap
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 5/2002, Volume 99, Issue 11, pp. 7548 - 7553
Journal Article
Journal Article