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Alternative mechanisms associated with silencing of CDKN1C in Beckwith–Wiedemann syndrome
Background: Mutations in the imprinted gene CDKN1C account for approximately 10% of Beckwith–Wiedemann syndrome (BWS) cases. Fibroblasts from BWS patients with loss of methylation (LOM) at the imprinting control region (ICR) KvDMR1 have reduced CDKN1C expression. Another group of BWS patients with d...
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| Asıl Yazarlar: | , , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
BMJ Group
2005
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1736119/ https://ncbi.nlm.nih.gov/pubmed/16061564 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2004.030593 |
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