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Expression of a novel splice variant of FRMD7 in developing human fetal brains that is upregulated upon the differentiation of NT2 cells

FRMD7 mutations are associated with X-linked idiopathic congenital nystagmus (ICN); however, the underlying mechanisms whereby mutations of FRMD7 lead to ICN remain unclear. In a previous study, the first FRMD7 splice variant (FRMD7-S) was cloned and identified, and FRMD7-S was hypothesized to play...

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書誌詳細
主要な著者: LI, YINGZHI, PU, JIALI, ZHANG, BAORONG
フォーマット: Artigo
言語:Inglês
出版事項: D.A. Spandidos 2014
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC4151643/
https://ncbi.nlm.nih.gov/pubmed/25187810
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/etm.2014.1916
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