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Bi-allelic loss-of-function variants in CLCN2 cause retinal degeneration via impairing phagocytosis in patient retinal pigment epithelium

GEO Series GSE216834. Homo sapiens. 6 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

Topics

Dataset details

Repository
geo
Published
October 1, 2025
License
GEO-Open
DOI
geo/GSE216834
Open full record on ShareScore ↗

Scored with release 0.9.0

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