Genome Medicine (Mar 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

  • Francesco Vetrini,
  • Shane McKee,
  • Jill A. Rosenfeld,
  • Mohnish Suri,
  • Andrea M. Lewis,
  • Kimberly Margaret Nugent,
  • Elizabeth Roeder,
  • Rebecca O. Littlejohn,
  • Sue Holder,
  • Wenmiao Zhu,
  • Joseph T. Alaimo,
  • Brett Graham,
  • Jill M. Harris,
  • James B. Gibson,
  • Matthew Pastore,
  • Kim L. McBride,
  • Makanko Komara,
  • Lihadh Al-Gazali,
  • Aisha Al Shamsi,
  • Elizabeth A. Fanning,
  • Klaas J. Wierenga,
  • Daryl A. Scott,
  • Ziva Ben-Neriah,
  • Vardiella Meiner,
  • Hanoch Cassuto,
  • Orly Elpeleg,
  • J. Lloyd Holder Jr,
  • Lindsay C. Burrage,
  • Laurie H. Seaver,
  • Lionel Van Maldergem,
  • Sonal Mahida,
  • Janet S. Soul,
  • Margaret Marlatt,
  • Ludmila Matyakhina,
  • Julie Vogt,
  • June-Anne Gold,
  • Soo-Mi Park,
  • Vinod Varghese,
  • Anne K. Lampe,
  • Ajith Kumar,
  • Melissa Lees,
  • Muriel Holder-Espinasse,
  • Vivienne McConnell,
  • Birgitta Bernhard,
  • Ed Blair,
  • Victoria Harrison,
  • The DDD study,
  • Donna M. Muzny,
  • Richard A. Gibbs,
  • Sarah H. Elsea,
  • Jennifer E. Posey,
  • Weimin Bi,
  • Seema Lalani,
  • Fan Xia,
  • Yaping Yang,
  • Christine M. Eng,
  • James R. Lupski,
  • Pengfei Liu

DOI
https://doi.org/10.1186/s13073-019-0630-1
Journal volume & issue
Vol. 11, no. 1
pp. 1 – 2

Abstract

Read online

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.