Aberrant splicing of tau pre-mRNA caused by intronic mutations associated with the inherited dementia frontotemporal dementia with parkinsonism linked to chromosome 17. [electronic resource]
Producer: 20000706Description: 4036-48 p. digitalISSN:- 0270-7306
- Adult
- Alternative Splicing
- Base Sequence
- Binding Sites
- Chromosomes, Human, Pair 17
- Dementia -- genetics
- Exons
- Frontal Lobe
- Genetic Linkage
- HeLa Cells
- Humans
- Introns
- Molecular Sequence Data
- Mutation
- Nucleic Acid Conformation
- Oligonucleotides
- Parkinsonian Disorders -- genetics
- RNA Precursors
- Ribonuclease H -- metabolism
- Ribonucleoprotein, U1 Small Nuclear -- metabolism
- Ribonucleoprotein, U4-U6 Small Nuclear -- metabolism
- Temporal Lobe
- tau Proteins -- genetics
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
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