Case report: "Major fetal cardiac pathology associated with a novel CTNND1 mutation"
BackgroundThe p120-ctn protein, encoded by CTNND1, is involved in intercellular connections and regulates epithelial-mesenchymal transformation. CTNND1 mutations can lead to blepharocheilodontic syndrome (BCDS). Increasing evidence shows that although BCDS mainly manifests as craniofacial and oral d...
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| Main Authors: | , , , , , , |
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| Format: | Book |
| Published: |
Frontiers Media S.A.,
2023-05-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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