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Microarray analysis of gene/transcript expression in Angelman syndrome: deletion versus UPD
Angelman syndrome (AS) is a neurodevelopmental disorder due to a functional deficit, usually a deletion, of the UBE3A gene located in the 15q11–q13 chromosome region. We report the first microarray analysis of gene expression in AS using a custom cDNA microarray to compare expression patterns from l...
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| Publicat a: | Genomics |
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| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2005
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6800218/ https://ncbi.nlm.nih.gov/pubmed/15607424 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ygeno.2004.10.010 |
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