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A new deletion refines the boundaries of the murine Prader–Willi syndrome imprinting center
The human chromosomal 15q11–15q13 region is subject to both maternal and paternal genomic imprinting. Absence of paternal gene expression from this region results in Prader–Willi syndrome (PWS), while absence of maternal gene expression leads to Angelman syndrome. Transcription of paternally express...
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| Asıl Yazarlar: | , , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Oxford University Press
2011
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3153308/ https://ncbi.nlm.nih.gov/pubmed/21659337 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddr262 |
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