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Whole Genome Microarray Analysis of Gene Expression in an Imprinting Center Deletion Mouse Model of Prader–Willi Syndrome
Prader–Willi syndrome (PWS) is caused by loss of paternally expressed genes in the 15q11-q13 region. To further characterize alterations in gene expression in this classical obesity syndrome we used whole genome microarrays to study a PWS mouse model resulting from a paternally derived imprinting ce...
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| 出版年: | Am J Med Genet A |
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| 主要な著者: | , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2007
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5453790/ https://ncbi.nlm.nih.gov/pubmed/17036336 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.31504 |
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