A single splice site mutation in human-specific ARHGAP11B causes basal progenitor amplification
Single nucleotide substitution played important role in evolutionary expansion of human neocortex.
| Main Authors: | , , , , |
|---|---|
| Format: | Online |
| Language: | English |
| Published: |
American Association for the Advancement of Science
2016
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| Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5142801/ |