ロード中...
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...
保存先:
| 主要な著者: | , , , |
|---|---|
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
The National Academy of Sciences
1998
|
| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC19156/ https://ncbi.nlm.nih.gov/pubmed/9465079 |
| タグ: |
タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!
|