Identification of a silencing element in the human 15q11-q13 imprinting center by using transgenic Drosophila
Prader–Willi syndrome (PWS) and Angelman syndrome are neurogenetic disorders caused by the lack of a paternal or a maternal contribution from human chromosome 15q11-q13, respectively. Deletions in the transcription unit of the imprinted SNRPN gene have been found in patients who have PWS or Angelman...
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| Izdano u: | Proc Natl Acad Sci U S A |
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| Glavni autori: | , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
National Academy of Sciences
1998
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC19156/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/9465079/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.95.4.1698 |
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