Article info

Original research
BTB domain mutations perturbing KCTD15 oligomerisation cause a distinctive frontonasal dysplasia syndrome

Authors

  1. Correspondence to Professor Alex N Bullock, Centre for Medicines Discovery, University of Oxford, Oxford OX3 7FZ, UK; alex.bullock{at}cmd.ox.ac.uk
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Citation

Miller KA, Cruz Walma DA, Pinkas DM, et al
BTB domain mutations perturbing KCTD15 oligomerisation cause a distinctive frontonasal dysplasia syndrome

Publication history

  • Received July 24, 2023
  • Accepted December 21, 2023
  • First published January 31, 2024.
Online issue publication 
April 19, 2024

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