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

Overview of attention for article published in Journal of Medical Genetics, January 2024

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In the top 25% of all research outputs scored by Altmetric
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RT @VerityCockbain: Great to be part of this fascinating story, mutations in new disease gene KCTD15 cause a distinctive frontonasal syndr…

RT @VerityCockbain: Great to be part of this fascinating story, mutations in new disease gene KCTD15 cause a distinctive frontonasal syndr…

RT @OxfordCranio: Read the latest collaboration from the @Wilkie_Lab @oxfordcranio Unit and colleagues in the Journal of Medical Genetics.…

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