Preliminary studies on parkin gene deletion at exons 1 to 6 in Chinese patients with praecox Parkinson's disease

Chinese Journal of Medical Genetics

Volumn 17, Issue 5, 2000, Pages 323-325

  Bai, H ^a   Shao, M ^a   Dong, X ^a   Yang, J ^a   Gao, Q ^a   Li, Y ^a   Chen, B ^a  

^a CAPITAL MEDICAL UNIVERSITY   (China)

Author keywords

Deletion mutation; Parkin gene; Parkinson's disease

Indexed keywords

AGAR GEL ELECTROPHORESIS; ARTICLE; ATHETOSIS; BRADYKINESIA; CHINA; CLINICAL ARTICLE; CLINICAL FEATURE; DATA ANALYSIS; EXON; EXTRACTION; GENE DELETION; GENE EXPRESSION; HUMAN; PARKINSON DISEASE; POLYMERASE CHAIN REACTION; RIGIDITY; TREMOR;

ADOLESCENT; ADULT; ENGLISH ABSTRACT; EXONS; FEMALE; GENE DELETION; HUMAN; LIGASES; MALE; MIDDLE AGE; PARKINSON DISEASE;

EID: 0033787310     PISSN: 10039406     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (7)

1. Genetics of Parkinson's disease
2. Mutation in the parkin gene cause autosomal recessive juvenile parkinsonism
3. Homozygous deletion in parkin gene in European and North Africa families with autosomal recessive juvenile parkinsonism
4. Point mutations (Thr204Arg and Ala311stop) in the parkin gene
5. Early-onset parkinsonism with diurnal fluctuation-clinical and pathological studies
6. Putting the parkin into Parkinson's disease
7. Ubiquitin, proteasome, and the regulation of intracellular protein degradation