Abstract
To investigate sequences or mutations associated with neurodegenerative disorders, we performed analyses for the NFAT5 gene, which is located in the candidate region for the autosomal dominantly inherited spinocerebellar ataxia type 4 (SCA4). PCR based expression analyses detected NFAT5 transcripts with alternative splicing in 27 fetal and adult human tissues. Interestingly, by using quantitative methods on cDNA from fetal and adult human brain a significant difference at the expression level for one splice form could be shown. Copyright (C) 2000 Elsevier Science B.V.
| Original language | English |
|---|---|
| Journal | Molecular Brain Research |
| Volume | 83 |
| Issue number | 1-2 |
| Pages (from-to) | 125-127 |
| Number of pages | 3 |
| ISSN | 0169-328X |
| DOIs | |
| Publication status | Published - 10.11.2000 |
Funding
This work was supported by the Fritz Thyssen Stiftung [AZ1999 2060] (Köln). We would like to thank Nina Richter for excellent technical assistance.
Research Areas and Centers
- Research Area: Medical Genetics