Genome Instability and Senescence Are Markers of Cornelia de Lange Syndrome Cells
Cornelia de Lange syndrome (CdLS) is a rare, dominantly inherited multisystem developmental disorder. Pathogenic variants in genes encoding the structural subunits and regulatory proteins of the cohesin complex (<i>NIPBL</i>, <i>SMC1A</i>, <i>SMC3</i>, <i>HD...
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| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
| Published: |
MDPI AG
2024-12-01
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| Series: | Cells |
| Subjects: | |
| Online Access: | https://www.mdpi.com/2073-4409/13/23/2025 |
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