A single splice site mutation in human-specific ARHGAP11B causes basal progenitor amplification Florio, M. ; Namba, T. ; Pa a bo, S. ; Hiller, M. ; Huttner, W. B. Abstract Publication: Science Advances Pub Date: December 2016 DOI: 10.1126/sciadv.1601941 Bibcode: 2016SciA....2E1941F