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Testing the effects of FSHD candidate gene expression in vertebrate muscle development

The genetic lesion leading to facioscapulohumeral muscular dystrophy (FSHD) is a dominant deletion at the 4q35 locus. The generally accepted disease model involves an epigenetic dysregulation in the region resulting in the upregulation of one or more proximal genes whose overexpression specifically...

詳細記述

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書誌詳細
主要な著者: Wuebbles, Ryan D, Long, Steven W, Hanel, Meredith L, Jones, Peter L
フォーマット: Artigo
言語:Inglês
出版事項: e-Century Publishing Corporation 2010
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC2872745/
https://ncbi.nlm.nih.gov/pubmed/20490329
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