Parkinson's genetics: An embarrassment of riches

Annals of Neurology

Volumn 51, Issue 1, 2002, Pages 7-8

  Gwinn Hardy, Katrina ^a,b   Farrer, Matt ^a  

^a NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE   (United States)

^b MAYO CLINIC   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

LEVODOPA;

ADULT; CHROMOSOMAL LOCALIZATION; CHROMOSOME 1P; CHROMOSOME ARM; DYSKINESIA; EDITORIAL; GENE LOCATION; GENETIC ANALYSIS; GENETIC LINKAGE; GENETIC VARIABILITY; HERITABILITY; HUMAN; PARKINSON DISEASE; PARKINSONISM; PRIORITY JOURNAL; PROTEIN DEGRADATION;

HUMANS; LINKAGE (GENETICS); PARKINSON DISEASE;

EID: 0036135131     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.10091     Document Type: Editorial

References (23)

1. Mutation in the alpha-synuclein gene identified in families with Parkinson's disease
2. Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism
3. The ubiquitin pathway in Parkinson's disease
4. Case-control study of the ubiquitin carboxy-terminal hydrolase L1 gene in Parkinson's disease
5. A chromosome 4p haplotype segregating with Parkinson's disease and postural tremor
6. A susceptibility locus for Parkinson's disease maps to chromosome 2p13
7. Location of a novel locus for autosomal recessive early-onset parkinsonism, PARK6, on human chromosome 1p35-p36
8. PARK7, a novel locus for autosomal recessive early-onset parkinsonism on chromosome 1p36
9. A susceptibility gene for late-onset idiopathic Parkinson's disease successfully mapped
10. Familial aggregation of Parkinson's disease in Iceland
11. α-Synuclein gene haplotypes are associated with Parkinson's disease
12. Increased susceptibility to sporadic Parkinson's disease by a certain combined alpha-synuclein/apolipoprotein E genotype
13. PARK6-Linked Parkinsonism Occurs in Several European Families
14. Identification of a novel primary torsion dystonia locus (DYT13) on chromosome 1p36 in an Italian family with cranial-cervical or upper limb onset
15. Association between early-onset Parkinson's disease and mutations in the parkin gene
16. Amyloid, the presenilins and Alzheimer's disease
17. Familial Parkinson disease gene, parkin, is a ubiquitin-protein ligase
18. Lewy bodies and parkinsonism in families with parkin mutations
19. Ubiquitination of a new form of alpha-synuclein by parkin from human brain: Implications for Parkinson's disease
20. Ubiquination-dependent mechanisms regulate synaptic growth and function
21. Synucleins in synaptic plasticity and neurodegenerative disorders
22. The sequence of the human genome
23. Initial sequencing and analysis of the human genome