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Prader-Willi Syndrome: Obesity due to Genomic Imprinting
Prader-Willi syndrome (PWS) is a complex neurodevelopmental disorder due to errors in genomic imprinting with loss of imprinted genes that are paternally expressed from the chromosome 15q11-q13 region. Approximately 70% of individuals with PWS have a de novo deletion of the paternally derived 15q11-...
שמור ב:
| מחבר ראשי: | |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Bentham Science Publishers Ltd
2011
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| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3137005/ https://ncbi.nlm.nih.gov/pubmed/22043168 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2174/138920211795677877 |
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