Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17. [electronic resource]
Producer: 19981124Description: 13103-7 p. digitalISSN:- 0027-8424
- Adult
- Age of Onset
- Aged
- Alternative Splicing
- Amino Acid Sequence
- Chromosome Mapping
- Chromosomes, Human, Pair 17
- Dementia -- genetics
- Genetic Linkage
- Globus Pallidus -- pathology
- Humans
- Introns
- Middle Aged
- Molecular Sequence Data
- Neurodegenerative Diseases -- genetics
- Parkinson Disease -- genetics
- Point Mutation
- Pons -- pathology
- Repetitive Sequences, Amino Acid
- Sequence Alignment
- Sequence Homology, Amino Acid
- Substantia Nigra -- pathology
- tau Proteins -- chemistry
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S.
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