Affordable Access

Access to the full text

Author Correction: A missense mutation in the HECT domain of NEDD4L identified in a girl with periventricular nodular heterotopia, polymicrogyria, and cleft palate

Authors
  • Kato, Koji
  • Miya, Fuyuki
  • Hori, Ikumi
  • Ieda, Daisuke
  • Ohashi, Kei
  • Negishi, Yutaka
  • Hattori, Ayako
  • Okamoto, Nobuhiko
  • Kato, Mitsuhiro
  • Tsunoda, Tatsuhiko
  • Yamasaki, Mami
  • Kanemura, Yonehiro
  • Kosaki, Kenjiro
  • Saitoh, Shinji
Type
Published Article
Journal
Journal of Human Genetics
Publisher
Springer Nature
Publication Date
Apr 26, 2019
Volume
64
Issue
7
Pages
701–702
Identifiers
DOI: 10.1038/s10038-019-0610-8
Source
Springer Nature
License
Yellow

Abstract

Since the publication of this article, it has been brought to our attention, that the identified mutation (NM_015277: c.2617 G > A; p.Glu873Lys) is identical with the mutation (NM_001144967: c.2677 G > A; p.Glu893Lys) reported by Broix et al (Nature Genetics 48, 1349–1358, 2016 10.1038/ng.3676). Therefore the mutation is not novel but recurrent. Accordingly, the word “novel” should be deleted throughout the article including the title. Thus, the title should read “A missense mutation in the HECT domain of NEDD4L identified in a girl with periventricular nodular heterotopia, polymicrogyria, and cleft palate.”

Report this publication

Statistics

Seen <100 times