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Biallelic variants in SNUPN cause a limb girdle muscular dystrophy with myofibrillar-like features

GEO Series GSE253519. Homo sapiens. 5 samples. Type: Expression profiling by high throughput sequencing.

ShareScore

20/100

Overall dataset sharing score

Score breakdown

These five areas show where the dataset supports — or may limit — practical reuse.

Stewardship
4
Harmonization
8
Access
0
Reuse readiness
0
Engagement
8

Topics