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. 2019 Mar 25;11:16. doi: 10.1186/s13073-019-0630-1

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 1,30, Shane McKee 2, Jill A Rosenfeld 3, Mohnish Suri 4, Andrea M Lewis 3, Kimberly Margaret Nugent 3,5, Elizabeth Roeder 3,5, Rebecca O Littlejohn 3,5, Sue Holder 6, Wenmiao Zhu 1, Joseph T Alaimo 3, Brett Graham 3,30, Jill M Harris 8, James B Gibson 8, Matthew Pastore 9, Kim L McBride 9, Makanko Komara 10, Lihadh Al-Gazali 10, Aisha Al Shamsi 11, Elizabeth A Fanning 12, Klaas J Wierenga 12,32, Daryl A Scott 3,31, Ziva Ben-Neriah 13, Vardiella Meiner 13, Hanoch Cassuto 28, Orly Elpeleg 29, J Lloyd Holder Jr 14, Lindsay C Burrage 3, Laurie H Seaver 15, Lionel Van Maldergem 16, Sonal Mahida 17, Janet S Soul 17, Margaret Marlatt 17, Ludmila Matyakhina 18, Julie Vogt 19, June-Anne Gold 20, Soo-Mi Park 20, Vinod Varghese 21, Anne K Lampe 22, Ajith Kumar 23, Melissa Lees 23, Muriel Holder-Espinasse 24, Vivienne McConnell 2, Birgitta Bernhard 6, Ed Blair 25, Victoria Harrison 26; The DDD study27, Donna M Muzny 3,7, Richard A Gibbs 3,7, Sarah H Elsea 1,3, Jennifer E Posey 3, Weimin Bi 1,3, Seema Lalani 1,3,14, Fan Xia 1,3, Yaping Yang 1,3, Christine M Eng 1,3, James R Lupski 1,3,7,14, Pengfei Liu 1,3,✉
PMCID: PMC6434874  PMID: 30909959

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

  • 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 free article] [PubMed] [Google Scholar]

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