Phenotypic continuum between Waardenburg syndrome and idiopathic hypogonadotropic hypogonadism in humans with SOX10 variants

Abstract

Correction to: Genetics in Medicine 2021; https://doi.org/10.1038/s41436-020-01051-3, published online 13 January 2021. In the article “Phenotypic continuum between Waardenburg syndrome and idiopathic hypogonadotropic hypogonadism in humans with SOX10 variants” by Rojas RA et al (Genet Med 2021;23:629-636), the author Kathryn B. Salnikov’s name was incorrectly listed as “Kathyrn B. Salnikov” in the author listing. The article has been corrected online and can be accessed at https://doi.org/10.1038/s41436-020-01051-3. The authors would like to apologize for any inconvenience this may have caused. Phenotypic continuum between Waardenburg syndrome and idiopathic hypogonadotropic hypogonadism in humans with SOX10 variantsGenetics in MedicineVol. 23Issue 4PreviewSOX10 variants previously implicated in Waardenburg syndrome (WS) have now been linked to Kallmann syndrome (KS), the anosmic form of idiopathic hypogonadotropic hypogonadism (IHH). We investigated whether SOX10-associated WS and IHH represent elements of a phenotypic continuum within a unifying disorder or if they represent phenotypically distinct allelic disorders. Full-Text PDF Open Archive