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Volumn 4, Issue 11, 2001, Pages 1061-1062
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A candidate gene for human neurodegenerative disorders: A rat PKCγ mutation causes a Parkinsonian syndrome
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Author keywords
[No Author keywords available]
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Indexed keywords
COMPLEMENTARY DNA;
ISOENZYME;
PROTEIN KINASE C;
PROTEIN KINASE C GAMMA;
UNCLASSIFIED DRUG;
ANIMAL CELL;
ANIMAL MODEL;
ANIMAL TISSUE;
ARTICLE;
CONTROLLED STUDY;
DEGENERATIVE DISEASE;
GENE MUTATION;
HISTOPATHOLOGY;
MUTANT;
NEUROPATHOLOGY;
NONHUMAN;
PARKINSONISM;
PRIORITY JOURNAL;
RAT;
SEQUENCE ANALYSIS;
SEQUENCE HOMOLOGY;
WILD TYPE;
ANIMALS;
BASE SEQUENCE;
CODON, NONSENSE;
CODON, TERMINATOR;
CROSSES, GENETIC;
DOPAMINE;
HUMANS;
IMMUNOHISTOCHEMISTRY;
ISOENZYMES;
LINKAGE (GENETICS);
MOLECULAR SEQUENCE DATA;
MUTATION;
NEURONS;
PARKINSONIAN DISORDERS;
PROTEIN KINASE C;
PURKINJE CELLS;
RATS;
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EID: 0035705226
PISSN: 10976256
EISSN: None
Source Type: Journal
DOI: 10.1038/nn740 Document Type: Article |
Times cited : (28)
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References (11)
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