Incomplete silencing of full mutation alleles in males with fragile X syndrome is associated with autistic features
出版年份 2019 全文链接
标题
Incomplete silencing of full mutation alleles in males with fragile X syndrome is associated with autistic features
作者
关键词
-
出版物
Molecular Autism
Volume 10, Issue 1, Pages -
出版商
Springer Science and Business Media LLC
发表日期
2019-05-03
DOI
10.1186/s13229-019-0271-7
参考文献
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- β-glucuronidase use as a single internal control gene may confound analysis in FMR1 mRNA toxicity studies
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