geoopen
Correction of splicing defect in compound heterozygous FRDA patient carrying FXN 165+5G>C point mutation.
GEO Series GSE262763. Homo sapiens. 1 samples. Type: Expression profiling by high throughput sequencing.
ShareScore
24/100
Overall dataset sharing score
Score breakdown
These five areas show where the dataset supports — or may limit — practical reuse.
- Stewardship
- 4
- Harmonization
- 8
- Access
- 4
- Reuse readiness
- 0
- Engagement
- 8