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.

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 syndrome.
Publication TypeJournal Article
Year of Publication2019
AuthorsVetrini, F, McKee, S, Rosenfeld, JA, Suri, M, Lewis, AM, Nugent, KMargaret, Roeder, E, Littlejohn, RO, Holder, S, Zhu, W, Alaimo, JT, Graham, B, Harris, JM, Gibson, JB, Pastore, M, McBride, KL, Komara, M, Al-Gazali, L, Shamsi, AAl, Fanning, EA, Wierenga, KJ, Scott, DA, Ben-Neriah, Z, Meiner, V, Cassuto, H, Elpeleg, O, J Holder, L, Burrage, LC, Seaver, LH, Van Maldergem, L, Mahida, S, Soul, JS, Marlatt, M, Matyakhina, L, Vogt, J, Gold, J-A, Park, S-M, Varghese, V, Lampe, AK, Kumar, A, Lees, M, Holder-Espinasse, M, McConnell, V, Bernhard, B, Blair, E, Harrison, V, Muzny, DM, Gibbs, RA, Elsea, SH, Posey, JE, Bi, W, Lalani, S, Xia, F, Yang, Y, Eng, CM, Lupski, JR, Liu, P
Corporate AuthorsDDD study
JournalGenome Med
Volume11
Issue1
Pagination16
Date Published2019 Mar 25
ISSN1756-994X
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.
DOI10.1186/s13073-019-0630-1
Alternate JournalGenome Med
PubMed ID30909959
PubMed Central IDPMC6434874
Grant ListK08 HG008986 / HG / NHGRI NIH HHS / United States
MC_PC_16018 / MRC_ / Medical Research Council / United Kingdom