Research ArticleGENETICS
A single splice site mutation in human-specific ARHGAP11B causes basal progenitor amplification
- 1Max Planck Institute of Molecular Cell Biology and Genetics, Pfotenhauerstraße 108, D-01307 Dresden, Germany.
- 2Max Planck Institute for Evolutionary Anthropology, Deutscher Platz 6, D-04103 Leipzig, Germany.
- 3Max Planck Institute for the Physics of Complex Systems, Noethnitzer Straße 38, D-01187 Dresden, Germany.
- ↵†Corresponding author. Email: huttner{at}mpi-cbg.de
↵* Present address: Department of Genetics, Harvard Medical School, Boston, MA 02115, USA.
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Science Advances 07 Dec 2016:
Vol. 2, no. 12, e1601941
DOI: 10.1126/sciadv.1601941
Vol. 2, no. 12, e1601941
DOI: 10.1126/sciadv.1601941
Marta Florio
Max Planck Institute of Molecular Cell Biology and Genetics, Pfotenhauerstraße 108, D-01307 Dresden, Germany.
Takashi Namba
Max Planck Institute of Molecular Cell Biology and Genetics, Pfotenhauerstraße 108, D-01307 Dresden, Germany.
Svante Pääbo
Max Planck Institute for Evolutionary Anthropology, Deutscher Platz 6, D-04103 Leipzig, Germany.
Michael Hiller
Max Planck Institute of Molecular Cell Biology and Genetics, Pfotenhauerstraße 108, D-01307 Dresden, Germany.Max Planck Institute for the Physics of Complex Systems, Noethnitzer Straße 38, D-01187 Dresden, Germany.
Wieland B. Huttner
Max Planck Institute of Molecular Cell Biology and Genetics, Pfotenhauerstraße 108, D-01307 Dresden, Germany.
