Correction: 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 Medicine (2019) 11 (12) DOI: 10.1186/s13073-019-0623-0)

Francesco Vetrini,Shane McKee,Jill A. Rosenfeld,Mohnish Suri,Andrea M. Lewis,Kimberly Nugent,Elizabeth Roeder,Rebecca O. Littlejohn,Sue Holder,Wenmiao Zhu,Joseph T. Alaimo,Brett H. 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,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 Kuttannair Kumar,Melissa Lees,Muriel Holder-Espinasse,Vivienne McConnell,Birgitta Bernhard,Ed Blair,Victoria Harrison,Donna M. Muzny,Richard A. Gibbs,Sarah H. Elsea,Jennifer E. Posey,Weimin Bi,Seema R. Lalani,Fan Xia,Yaping Yang,Christine M. Eng,James R. Lupski,Pengfei Liu

Genome Medicine（2019）

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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.

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Key words

pathogenic variants,smith–magenis syndrome,neurological impairments,intellectual disability

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