Research ArticleGENETICS

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

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Science Advances  07 Dec 2016:
Vol. 2, no. 12, e1601941
DOI: 10.1126/sciadv.1601941

Article Information

vol. 2 no. 12

Online ISSN: 
History: 
  • Received for publication August 16, 2016
  • Accepted for publication November 3, 2016

Author Information

  1. Marta Florio1,*,
  2. Takashi Namba1,
  3. Svante Pääbo2,
  4. Michael Hiller1,3 and
  5. Wieland B. Huttner1,
  1. 1Max Planck Institute of Molecular Cell Biology and Genetics, Pfotenhauerstraße 108, D-01307 Dresden, Germany.
  2. 2Max Planck Institute for Evolutionary Anthropology, Deutscher Platz 6, D-04103 Leipzig, Germany.
  3. 3Max Planck Institute for the Physics of Complex Systems, Noethnitzer Straße 38, D-01187 Dresden, Germany.
  1. Corresponding author. Email: huttner{at}mpi-cbg.de
    • * Present address: Department of Genetics, Harvard Medical School, Boston, MA 02115, USA.

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