Additional file 1 of A novel KDM5C mutation associated with intellectual disability: molecular mechanisms and clinical implications

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Publication Details

Journal
Figshare
Published
2025-01-01
DOI
https://doi.org/10.6084/m9.figshare.28415525
Primary Topic
Genomics and Rare Diseases
Type
article
Field-Weighted Citation Impact
0.00
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article

Additional file 1 of A novel KDM5C mutation associated with intellectual disability: molecular mechanisms and clinical implications

Figshare
Genomics and Rare Diseases
article

Additional file 1 of A novel KDM5C mutation associated with intellectual disability: molecular mechanisms and clinical implications

article en

Abstract

No abstract available for this paper.
Figshare
Tongji University (CN)
Quality Education
Openalex Percentile: Top 55%
Genomics and Rare Diseases
DOIOpen Access PDFOpenAlex
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Additional file 1 of A novel KDM5C mutation associated with intellectual disability: molecular mechanisms and clinical implications · Figshare (2025) | TGRS Research Map | TGRS