2016·Science advances
A single splice site mutation in human-specific <i>ARHGAP11B</i> causes basal progenitor amplification
Florio MPapers in this archive, Namba TPapers in this archive, Pääbo SPapers in this archive, Hiller MPapers in this archive, Huttner WBPapers in this archive
Abstract
Single nucleotide substitution played important role in evolutionary expansion of human neocortex. Keywords: ARHGAP11B, neocortical expansion, human evolution, basal progenitors, neurogenesis, gene duplication, neocortex, brain size, RhoGAP, human-specific gene
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