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Published Erratum
, 11 (1), 16

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

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Published Erratum

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

Francesco Vetrini et al. Genome Med.

Abstract

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.

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References

    1. 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. doi: 10.1186/s13073-019-0623-0. - DOI - PMC - PubMed

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