zenodorestricted
raw data for "Two novel CACNA1F gene mutations cause two different phenotypes: Aland Eye Disease and Incomplete Congenital Stationary Night Blindness"
<p>DNA and mRNA sequences of two patients affected by CSNB2</p>
ShareScore
4/100
Overall dataset sharing score
Score breakdown
These five areas show where the dataset supports — or may limit — practical reuse.
- Stewardship
- 4
- Harmonization
- 0
- Access
- 0
- Reuse readiness
- 0
- Engagement
- 0