Author Correction: Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders (Nature Communications, (2020), 11, 1, (4932), 10.1038/s41467-020-18723-y)

T Wang; K Hoekzema; D Vecchio; H Wu; A Sulovari; BP Coe; MA Gillentine; AB Wilfert; LA Perez-Jurado; M Kvarnung; Y Sleyp; RK Earl; JA Rosenfeld; MR Geisheker; L Han; B Du; C Barnett; E Thompson; M Shaw; R Carroll; K Friend; R Catford; EE Palmer; X Zou; J Ou; H Li; H Guo; J Gerdts; E Avola; G Calabrese; M Elia; D Greco; A Lindstrand; A Nordgren; BM Anderlid; G Vandeweyer; A Van Dijck; N Van der Aa; B McKenna; M Hancarova; S Bendova; M Havlovicova; G Malerba; BD Bernardina; P Muglia; A van Haeringen; MJV Hoffer; B Franke; G Cappuccio; M Delatycki; PJ Lockhart; MA Manning; P Liu; IE Scheffer; N Brunetti-Pierri; N Rommelse; DG Amaral; GWE Santen; E Trabetti; Z Sedláček; JJ Michaelson; K Pierce; E Courchesne; RF Kooy; J Acampado; AJ Ace; A Amatya; I Astrovskaya; A Bashar; E Brooks; ME Butler; LA Cartner; W Chin; WK Chung; AM Daniels; P Feliciano; C Fleisch; S Ganesan; W Jensen; AE Lash; R Marini; VJ Myers; E O’Connor; C Rigby; BE Robertson; N Shah; S Shah; E Singer; LAG Snyder; AN Stephens; J Tjernagel; BM Vernoia; N Volfovsky; LC White; A Hsieh; Y Shen; X Zhou; TN Turner; E Bahl; TR Thomas

Journal article

Author Correction: Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders (Nature Communications, (2020), 11, 1, (4932), 10.1038/s41467-020-18723-y)

T Wang, K Hoekzema, D Vecchio, H Wu, A Sulovari, BP Coe, MA Gillentine, AB Wilfert, LA Perez-Jurado, M Kvarnung, Y Sleyp, RK Earl, JA Rosenfeld, MR Geisheker, L Han, B Du, C Barnett, E Thompson, M Shaw, R Carroll Show all

Nature Communications | NATURE RESEARCH | Published : 2020

DOI: 10.1038/s41467-020-19289-5

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Abstract

The original version of this Article contained an error on page 5 of the Results section, which incorrectly read ‘They are characterized by craniofacial dysmorphisms (9/10), thin vermillion border and lips (4/7), and feeding difficulties (6/11), and exhibit neonatal hypotonia (10/7)’. The correct version states ‘They are characterized by craniofacial dysmorphisms (9/10), thin vermillion border and lips (4/7), and feeding difficulties (6/11), and exhibit neonatal hypotonia (7/10)’.