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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

Crossref DOI link: https://doi.org/10.1186/s13073-019-0630-1

Published Online: 2019-03-25

Published Print: 2019-12

Update policy: https://doi.org/10.1007/springer_crossmark_policy

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