PARK7, a novel locus for autosomal recessive early-onset parkinsonism, on chromosome 1p36

American Journal of Human Genetics

Volumn 69, Issue 3, 2001, Pages 629-634

  Van Duijn, C M ^a   Dekker, M C J ^a   Bonifati, V ^a,b   Galjaard, R J ^a   Houwing Duistermaat, J J ^a   Snijders, P J L M ^a   Testers, L ^a   Breedveld, G J ^a   Horstink, M ^c   Sandkuijl, L A ^a   Van Swieten, J C ^a   Oostra, B A ^a   Heutink, P ^a  

^a ERASMUS MEDICAL CENTER   (Netherlands)

^b SAPIENZA UNIVERSITY OF ROME   (Italy)

^c RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

DJ 1 PROTEIN; GENE PRODUCT; PARKIN; PROTEIN; PROTEIN PARK6; UNCLASSIFIED DRUG;

ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; AUTOSOMAL RECESSIVE INHERITANCE; CENTROMERE; CHROMOSOME 1P; CONSANGUINITY; DISEASE ASSOCIATION; GENE ISOLATION; GENE LOCUS; GENE MAPPING; GENE MUTATION; GENETIC ANALYSIS; GENETIC LINKAGE; HAPLOTYPE; HEREDITY; HOMOZYGOSITY; HUMAN; MARKER GENE; ONSET AGE; PARKINSON DISEASE; PARKINSONISM; PRIORITY JOURNAL;

EID: 0034892917     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/322996     Document Type: Article

References (16)

1. A wide variety of mutations in the Parkin gene are responsible for autosomal recessive parkinsonism in Europe: French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease
2. Unified Parkinson's disease rating scale
3. A chromosome 4p haplotype segregating with Parkinson's disease and postural tremor
4. A susceptibility locus for Parkinson's disease maps to chromosome 2p13
5. Parkinsonism: Onset, progression and mortality
6. Mutations in the Parkin gene cause autosomal recessive juvenile parkinsonism
7. Rapid multipoint linkage analysis of recessive traits in nuclear families, including homozygosity mapping
8. Homozygosity mapping: A way to map human recessive traits with the DNA of inbred children
9. Genetic dissection of complex traits: Guidelines for interpreting and reporting linkage results
10. The ubiquitin pathway in Parkinson's disease
11. Association between early-onset Parkinson's disease and mutations in the Parkin gene: French Parkinson's Disease Genetics Study Group
12. Pitfalls in homozygosity mapping
13. A simple salting out procedure for extracting DNA from human nucleated cells
14. Mutation in the α-synuclein gene identified in families with Parkinson's disease
15. Levodopa-responsive dystonia. GTP cyclohydrolase I or Parkin mutations?
16. Localization of a novel locus for autosomal recessive early-onset parkinsonism, PARK6, on human chromosome 1p35-p36