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 Med. 2019 Mar 25;11(1):16.
doi: 10.1186/s13073-019-0630-1.
4 Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA.
5 Nottingham Genetics Service, Nottingham City Hospital, Nottingham, UK.
6 Department of Pediatrics, Baylor College of Medicine, San Antonio, TX, 78207, USA.
7 North West Thames Regional Genetics Service, 759 Northwick Park Hospital, London, UK.
8 Dell Children's Medical Group, Austin, TX, 78723, USA.
9 Division of Genetic and Genomic Medicine, Nationwide Children's Hospital; and Department of Pediatrics, College of Medicine, Ohio State University, Columbus, OH, 43205, USA.
10 Department of Pediatrics, College of Medicine & Health Sciences, United Arab University, Al Ain, UAE.
11 Department of Pediatrics, Tawam Hospital, Al-Ain, UAE.
12 Department of Pediatrics, Section of Genetics, University of Oklahoma Health Sciences Center, Oklahoma City, OK, 73104, USA.
13 Present address: Mayo Clinic Florida, Department of Clinical Genomics, Jacksonville, FL, 32224, USA.
14 Department of Molecular Physiology and Biophysics, Baylor College of Medicine, Houston, TX, 77030, USA.
15 Department of Human Genetics and Metabolic Diseases, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.
16 The Hebrew University of Jerusalem, Jerusalem, Israel.
17 Monique and Jacques Roboh Department of Genetic Research, Hadassah-Hebrew University Medical Center, 91120, Jerusalem, Israel.
18 Department of Pediatrics, Texas Children's Hospital, Houston, TX, 77030, USA.
19 Department of Pediatrics, University of Hawaii, Honolulu, HI, 96826, USA.
20 Centre de Génétique Humaine, Université de Franche-Comté, Besançon, France.
21 Department of Neurology, Boston Children's Hospital, Boston, MA, 0211, USA.
22 Gene DX, Gaithersburg, MD, 20877, USA.
23 West Midlands Regional Clinical Genetics Service and Birmingham Health Partners, Women's and Children's Hospitals NHS Foundation Trust, Birmingham, UK.
24 East Anglia Regional Genetics Service, Addenbrooke's Hospital, Cambridge, UK.
25 All-Wales Medical Genetics Service, University Hospital of Wales, Cardiff, UK.
26 South East of Scotland Clinical Genetic Service, Western General Hospital, Edinburgh, UK.
27 North East Thames Regional Genetics Service, Great Ormond Street Hospital, London, UK.
28 South East Thames Regional Genetics Service, Guy's Hospital, London, UK.
29 Oxford Regional Genetics Service, Oxford University Hospitals, Oxford, UK.
30 Wessex Clinical Genetics Service, Princess Anne Hospital, Southampton, UK.
31 Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, 77030, USA.
32 Baylor Genetics, Houston, TX, 77021, USA. pengfeil@bcm.edu.
33 Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA. pengfeil@bcm.edu.
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.