Parkin and parkinson disease

Clinical Chemistry

Volumn 58, Issue 8, 2012, Pages 1260-1261

  Shimura, Hideki ^a   Mizuno, Yoshikuni ^a,b   Hattori, Nobutaka ^a  

^a JUNTENDO UNIVERSITY   (Japan)

^b KITASATO UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA SYNUCLEIN; AMYLOID BETA PROTEIN[1-42]; ATAXIN 3; BETA TUBULIN; PARKIN; POLYGLUTAMINE; POLYUBIQUITIN; UBIQUITIN CONJUGATING ENZYME; UBIQUITIN PROTEIN LIGASE E3;

ACTIN FILAMENT; AUTOSOMAL RECESSIVE DISORDER; CORRELATION ANALYSIS; GENE MUTATION; GENETIC ANALYSIS; GENETIC ASSOCIATION; HUMAN; LEWY BODY; NOTE; PARKINSON DISEASE; PATHOGENESIS; PROTEIN ANALYSIS;

HISTORY, 20TH CENTURY; HUMANS; MUTATION; PARKINSON DISEASE; UBIQUITIN-PROTEIN LIGASES;

EID: 84864479135     PISSN: 00099147     EISSN: 15308561     Source Type: Journal    
DOI: 10.1373/clinchem.2012.187054     Document Type: Note

References (4)

1. Yamamura Y, Sobue I, Ando K, Iida M, Yanagi T. Paralysis agitans of early onset with marked diurnal fluctuation of symptoms. Neurology 1973;23:239-44.
2. Matsumine H, Saito M, Shimoda-Matsubayashi S, Tanaka H, Ishikawa A, Nakagawa-Hattori Y, et al. Localization of a gene for an autosomal recessive form of juvenile Parkinsonism to chromosome 6q25.2-27. Am J Hum Genet 1997;60:588-96. (Pubitemid 27097607)
3. Kitada T, Asakawa S, Hattori N, Matsumine H, Yamamura Y, Minoshima S, et al. Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism. Nature 1998;392:605-8. (Pubitemid 28207717)
4. Shimura H, Hattori N, Kubo S, Yoshikawa M, Kitada T, Matsumine H, et al. Immunohistochemical and subcellular localization of Parkin protein: absence of protein in autosomal recessive juvenile parkinsonism patients. Ann Neurol 1999;45:668-72. (Pubitemid 29217599)