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KRIT1 heterozygous mutations are sufficient to induce a pathological phenotype in patient-derived iPSC models of Cerebral Cavernous Malformation

GEO Series GSE291768. Homo sapiens. 18 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