Association studies of Parkinson's disease and parkin polymorphisms [2]

Annals of Neurology

Volumn 48, Issue 1, 2000, Pages 126-127

  Klein, Christine ^a   Schumacher, Kirsten ^a   Jacobs, Helfried ^a   Hagenah, Johann ^a   Kis, Bernhard ^a,b   Garrels, Jennifer ^a   Schwinger, Eberhard ^a   Ozelius, Laurie ^c   Pramstaller, Peter ^b   Vieregge, Peter ^a   Kramer, Patricia L ^d  

^a UNIVERSITY OF LÜBECK   (Germany)

^b Department of Neurology   (Italy)

^c ALBERT EINSTEIN COLLEGE OF MEDICINE   (United States)

^d OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

AGAR GEL ELECTROPHORESIS; DISEASE ASSOCIATION; GENE; GENE FREQUENCY; GENE MUTATION; GENETIC POLYMORPHISM; HUMAN; LETTER; NEUROLOGIC EXAMINATION; PARKINSON DISEASE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL;

EID: 0033946025     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/1531-8249(200007)48:1<126::aid-ana22>3.0.co;2-k     Document Type: Letter

References (5)

1. Kitada T, Asakawa S, Hattori N, et al. Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism. Nature 1998;392:605-608
2. Wang M, Hattori N, Matsumine H, et al. Polymorphism in the parkin gene in sporadic Parkinson's disease. Ann Neurol 1999; 45:655-658
3. Satoh J-I, Kuroda Y. Association of codon 167 Ser/Asn heterozygosity in the parkin gene with sporadic Parkinson's disease. Neuroreport 1999;10:2735-2739
4. Gibb WRG, Lees AJ. The relevance of the Lewy body to the pathogenesis of idiopathic Parkinson's disease. J Neurol Neurosurg Psychiatry 1988;51:745-752
5. Tanner CM, Ottmann R, Goldman SM, et al. Parkinson's disease in twins: an etiologic study. JAMA 1999;281:341-346