SOX11 variants cause a neurodevelopmental disorder with infrequent ocular malformations and hypogonadotropic hypogonadism and with distinct DNA methylation profile

  • University of Washington Center for Mendelian Genomics (UW-CMG)
  • , Genomics England Research Consortium

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

27 Citations (Scopus)

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Biochemistry, Genetics and Molecular Biology