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Dataset related to article" Missing the pathological expansion in Huntington disease: de novo c.51C>G variant on the expanded allele causing intrafamilial allele dropout"

<p>DATASET CONTAINS&nbsp;Sanger sequencing data of the c.51C&gt;G variant in <em>HTT</em> gene.</p>

ShareScore

12/100

Overall dataset sharing score

Score breakdown

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

Stewardship
8
Harmonization
0
Access
0
Reuse readiness
0
Engagement
4

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