A single splice site mutation in human-specific ARHGAP11B causes basal progenitor amplification

标题
A single splice site mutation in human-specific ARHGAP11B causes basal progenitor amplification
作者
关键词
-
出版物
Science Advances
Volume 2, Issue 12, Pages e1601941-e1601941
出版商
American Association for the Advancement of Science (AAAS)
发表日期
2016-12-08
DOI
10.1126/sciadv.1601941

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