换一批
换一批Disease-causing 7.4 kb cis-regulatory deletion disrupting conserved non-coding sequences and their interaction with the FOXL2 promotor: implications for mutation screening.
作者：
主题词
5'非翻译区(5' Untranslated Regions);睑裂狭小(Blepharophimosis);细胞系(Cell Line);保守序列(Conserved Sequence);DNA突变分析(DNA Mutational Analysis);叉头转录因子类(Forkhead Transcription Factors);人类(Humans);启动区, 遗传(Promoter Regions, Genetic);蛋白质结合(Protein Binding);调控序列, 核酸(Regulatory Sequences, Nucleic Acid);序列缺失(Sequence Deletion)
DOI
10.1371/journal.pgen.1000522
PMID
19543368
发布时间
2021-10-20
- 浏览28
PLoS genetics
e1000522页
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