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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...

詳細記述

保存先:
書誌詳細
出版年:Genomics
主要な著者: Bittel, Douglas C., Kibiryeva, Nataliya, Talebizadeh, Zohreh, Driscoll, Daniel J., Butler, Merlin G.
フォーマット: Artigo
言語:Inglês
出版事項: 2005
主題:
オンライン・アクセス: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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