Correction to: Genome Med (2019) 11:12
https://doi.org/10.1186/s13073-019-0623-0
It was highlighted that the original article [1] contained a typographical error in the Results section. Subject 17 was incorrectly cited as Subject 1. This Correction article shows the revised statement. The original article has been updated.
Correct statement:
“Of note, subject 17 of our cohort presented with mild delayed motor milestones, generalized hypotonia, and, in particular, dysmorphic features including midface hypoplasia, tented upper lips, along with sleep issues, ASD, food-seeking behavior, and aggressive behavior; these clinical features are similar to those reported in SMS.”
Reference
Vetrini F, et al. De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith–Magenis syndrome. Genome Med. 2019;11:12. https://doi.org/10.1186/s13073-019-0623-0.
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Vetrini, F., McKee, S., Rosenfeld, J.A. et al. Correction to: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith–Magenis syndrome. Genome Med 11, 16 (2019). https://doi.org/10.1186/s13073-019-0630-1
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DOI: https://doi.org/10.1186/s13073-019-0630-1