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]
- Molecular and cellular biology Jun 2000
- 4036-48 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
0270-7306
10.1128/MCB.20.11.4036-4048.2000 doi
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