Fetal overgrowth in the Cdkn1c mouse model of Beckwith-Wiedemann syndrome
SUMMARY Mutations in the imprinted CDKN1C gene are associated with the childhood developmental disorder Beckwith-Wiedemann syndrome (BWS). Multiple mouse models with deficiency of Cdkn1c recapitulate some aspects of BWS but do not exhibit overgrowth of the newborn, a cardinal feature of patients wit...
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| Principais autores: | , , |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
The Company of Biologists
2011-11-01
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| Serier: | Disease Models & Mechanisms |
| Online adgang: | http://dmm.biologists.org/content/4/6/814 |
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