Article
The NIK protein kinase and C17orf1 genes: chromosomal mapping, gene structures and mutational screening in frontotemporal dementia and parkinsonism linked to chromosome 17.
Human genetics - 1 Sept 1998
Aronsson F C, Magnusson P, Andersson B, Karsten S L, Shibasaki Y, Lendon C L, Goate A M, Brookes A J
Abstract excerpt
Full exon-intron structures are presented for the NIK serine/threonine protein kinase gene and a novel gene termed C17orf1. By in situ hybridisation and radiation hybrid mapping, a cosmid (cDD-Z) that contains regions of both of these genes has been localised between markers D17S800 and D17S791 a...
Topics
- Carrier Proteins
- Chromosome Mapping
- Chromosomes, Human, Pair 17
- Cloning, Molecular
- DNA Primers
- Dementia
- Exons
- Humans
- Introns
- Mutation
- Parkinson Disease
- Protein Serine-Threonine Kinases
- NF-kappaB-Inducing Kinase