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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dc.contributor.authorVetrini, Francesco
dc.contributor.authorMcKee, Shane
dc.contributor.authorRosenfeld, Jill A.
dc.contributor.authorSuri, Mohnish
dc.contributor.authorLewis, Andrea M.
dc.contributor.authorNugent, Kimberly Margaret
dc.contributor.authorRoeder, Elizabeth
dc.contributor.authorLittlejohn, Rebecca O.
dc.contributor.authorHolder, Sue
dc.contributor.authorZhu, Wenmiao
dc.contributor.authorAlaimo, Joseph T.
dc.contributor.authorGraham, Brett
dc.contributor.authorHarris, Jill M.
dc.contributor.authorGibson, James B.
dc.contributor.authorPastore, Matthew
dc.contributor.authorMcBride, Kim L.
dc.contributor.authorKomara, Makanko
dc.contributor.authorAl-Gazali, Lihadh
dc.contributor.authorAl Shamsi, Aisha
dc.contributor.authorFanning, Elizabeth A.
dc.contributor.authorWierenga, Klaas J.
dc.contributor.authorScott, Daryl A.
dc.contributor.authorBen-Neriah, Ziva
dc.contributor.authorMeiner, Vardiella
dc.contributor.authorCassuto, Hanoch
dc.contributor.authorElpeleg, Orly
dc.contributor.authorLloyd Holder Jr, J.
dc.contributor.authorBurrage, Lindsay C.
dc.contributor.authorSeaver, Laurie H.
dc.contributor.authorVan Maldergem, Lionel
dc.contributor.authorMahida, Sonal
dc.contributor.authorSoul, Janet S.
dc.contributor.authorMarlatt, Margaret
dc.contributor.authorMatyakhina, Ludmila
dc.contributor.authorVogt, Julie
dc.contributor.authorGold, June-Anne
dc.contributor.authorPark, Soo-Mi
dc.contributor.authorVarghese, Vinod
dc.contributor.authorLampe, Anne K.
dc.contributor.authorKumar, Ajith
dc.contributor.authorLees, Melissa
dc.contributor.authorHolder-Espinasse, Muriel
dc.contributor.authorMcConnell, Vivienne
dc.contributor.authorBernhard, Birgitta
dc.contributor.authorBlair, Ed
dc.contributor.authorHarrison, Victoria
dc.contributor.authorMuzny, Donna M.
dc.contributor.authorGibbs, Richard A.
dc.contributor.authorElsea, Sarah H.
dc.contributor.authorPosey, Jennifer E.
dc.contributor.authorBi, Weimin
dc.contributor.authorLalani, Seema
dc.contributor.authorXia, Fan
dc.contributor.authorYang, Yaping
dc.contributor.authorEng, Christine M.
dc.contributor.authorLupski, James R.
dc.contributor.authorLiu, Pengfei
dc.contributor.departmentMedical and Molecular Genetics, School of Medicineen_US
dc.date.accessioned2019-08-07T18:38:32Z
dc.date.available2019-08-07T18:38:32Z
dc.date.issued2019-03-25
dc.description.abstractIt 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.en_US
dc.identifier.citationVetrini, F., McKee, S., Rosenfeld, J. A., Suri, M., Lewis, A. M., Nugent, K. M., … Liu, P. (2019). 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 medicine, 11(1), 16. doi:10.1186/s13073-019-0630-1en_US
dc.identifier.urihttps://hdl.handle.net/1805/20236
dc.language.isoen_USen_US
dc.publisherBiomed Centralen_US
dc.relation.isversionof10.1186/s13073-019-0630-1en_US
dc.relation.journalGenome Medicineen_US
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/us/*
dc.sourcePMCen_US
dc.subjectCorrectionsen_US
dc.titleCorrection to: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndromeen_US
dc.typeArticleen_US
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