Autosomal recessive juvenile parkinsonism: A key to understanding nigral degeneration in sporadic Parkinson's disease

Neuropathology

Volumn 20, Issue SUPPL., 2000, Pages 85-90

  Hattori, Nobutaka ^a   Shimura, Hideki ^a   Kubo, Shin Ichiro ^a   Kitada, Tohru ^a   Wang, Mei ^a   Asakawa, Shuichi ^b   Minashima, Shinsei ^b   Shimizu, Nobuyoshi ^b   Suzuki, Toshiaki ^c   Tanaka, Keiji ^d   Mizuno, Yoshikuni ^a  

^a JUNTENDO UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^b KEIO UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^c TOKYO METROPOLITAN INSTITUTE OF MEDICAL SCIENCE   (Japan)

^d JAPAN SCIENCE AND TECHNOLOGY AGENCY   (Japan)

Author keywords

Familial Parkinson's disease; Genetic factor; Lewy bodies; Parkin; Ubiquitin carboxy terminal hydrolase L1; Ubiquitin pathway; synuclein

Indexed keywords

ALPHA SYNUCLEIN; UBIQUITIN CONJUGATING ENZYME;

AUTOSOMAL RECESSIVE DISORDER; CELL DEATH; CLINICAL FEATURE; DISEASE COURSE; GENE MUTATION; GENETIC PREDISPOSITION; HUMAN; JUVENILE; LEWY BODY; ONSET AGE; PARKINSONISM; PATHOGENESIS; POSITRON EMISSION TOMOGRAPHY; PRIORITY JOURNAL; REVIEW; SUBSTANTIA NIGRA;

EID: 0033772662     PISSN: 09196544     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1440-1789.2000.00312.x     Document Type: Review

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