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ArticleJCI insight2026

Aebp1 loss in osteoprogenitors leads to skeletal defects resembling Ehlers-Danlos Syndrome by diminishing Wnt/β-catenin signaling.

Shuhao Feng et al.PubMed ↗Full text ↗Publisher ↗

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1 paper cites it

2026
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Full record →Abstract, authors, funding and every citing paper · PMID 41231548