De novo and rare inherited mutations implicate the transcriptional coregulator TCF20/SPBP in autism spectrum disorder.

  • Christian Babbs
  • , Deborah Lloyd
  • , Alistair T Pagnamenta
  • , Stephen R F Twigg
  • , Joanne Green
  • , Simon J McGowan
  • , Ghazala Mirza
  • , Rebecca Naples
  • , Vikram P Sharma
  • , Emanuela V Volpi
  • , Veronica J Buckle
  • , Steven A Wall
  • , Samantha J L Knight
  • , Jeremy R Parr
  • , Andrew O M Wilkie

    Research output: Contribution to journal › Article › peer-review

    Fingerprint

    Dive into the research topics of 'De novo and rare inherited mutations implicate the transcriptional coregulator TCF20/SPBP in autism spectrum disorder.'. Together they form a unique fingerprint.
    Sort by

    Biochemistry, Genetics and Molecular Biology