Erratum: De novo missense variants in exon 9 of SEPHS1 cause a neurodevelopmental condition with developmental delay, poor growth, hypotonia, and dysmorphic features (The American Journal of Human Genetics (2024) 111(4) (778–790), (S0002929724000739), (10.1016/j.ajhg.2024.02.016))

  • Care4Rare Canada Consortium
  • , Undiagnosed Diseases Network

Research output: Contribution to journal › Comment/debate › peer-review

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Medicine and Dentistry

Biochemistry, Genetics and Molecular Biology