geoopen
Loss-of-function mutations TDRD7 lead to a rare novel syndrome combining congenital cataract and non-obstructive azoospermia in humans
GEO Series GSE100019. Homo sapiens. 1 samples. Type: Genome variation profiling by SNP array.
ShareScore
12/100
Overall dataset sharing score
Score breakdown
These five areas show where the dataset supports — or may limit — practical reuse.
- Stewardship
- 4
- Harmonization
- 4
- Access
- 0
- Reuse readiness
- 0
- Engagement
- 4