Author Correction: A missense mutation in the HECT domain of NEDD4L identified in a girl with periventricular nodular heterotopia, polymicrogyria, and cleft palate (Journal of Human Genetics, (2017), 62, 9, (861-863), 10.1038/jhg.2017.53)

Koji Kato; Fuyuki Miya; Ikumi Hori; Daisuke Ieda; Kei Ohashi; Yutaka Negishi; Ayako Hattori; Nobuhiko Okamoto; Mitsuhiro Kato; Tatsuhiko Tsunoda; Mami Yamasaki; Yonehiro Kanemura; Kenjiro Kosaki; Shinji Saitoh

doi:10.1038/s10038-019-0610-8

Author Correction: A missense mutation in the HECT domain of NEDD4L identified in a girl with periventricular nodular heterotopia, polymicrogyria, and cleft palate (Journal of Human Genetics, (2017), 62, 9, (861-863), 10.1038/jhg.2017.53)

Koji Kato, Fuyuki Miya, Ikumi Hori, Daisuke Ieda, Kei Ohashi, Yutaka Negishi, Ayako Hattori, Nobuhiko Okamoto, Mitsuhiro Kato, Tatsuhiko Tsunoda, Mami Yamasaki, Yonehiro Kanemura, Kenjiro Kosaki, Shinji Saitoh

Research output: Contribution to journal › Comment/debate › peer-review

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 https://doi.org/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”.

Original language	English
Pages (from-to)	701-702
Number of pages	2
Journal	Journal of Human Genetics
Volume	64
Issue number	7
DOIs	https://doi.org/10.1038/s10038-019-0610-8
Publication status	Published - Jul 1 2019
Externally published	Yes

All Science Journal Classification (ASJC) codes

Genetics
Genetics(clinical)

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Kato, K., Miya, F., Hori, I., Ieda, D., Ohashi, K., Negishi, Y., Hattori, A., Okamoto, N., Kato, M., Tsunoda, T., Yamasaki, M., Kanemura, Y., Kosaki, K., & Saitoh, S. (2019). Author Correction: A missense mutation in the HECT domain of NEDD4L identified in a girl with periventricular nodular heterotopia, polymicrogyria, and cleft palate (Journal of Human Genetics, (2017), 62, 9, (861-863), 10.1038/jhg.2017.53). Journal of Human Genetics, 64(7), 701-702. https://doi.org/10.1038/s10038-019-0610-8

Author Correction: A missense mutation in the HECT domain of NEDD4L identified in a girl with periventricular nodular heterotopia, polymicrogyria, and cleft palate (Journal of Human Genetics, (2017), 62, 9, (861-863), 10.1038/jhg.2017.53). / Kato, Koji; Miya, Fuyuki; Hori, Ikumi et al.
In: Journal of Human Genetics, Vol. 64, No. 7, 01.07.2019, p. 701-702.

Research output: Contribution to journal › Comment/debate › peer-review

Kato, K, Miya, F, Hori, I, Ieda, D, Ohashi, K, Negishi, Y, Hattori, A, Okamoto, N, Kato, M, Tsunoda, T, Yamasaki, M, Kanemura, Y, Kosaki, K & Saitoh, S 2019, 'Author Correction: A missense mutation in the HECT domain of NEDD4L identified in a girl with periventricular nodular heterotopia, polymicrogyria, and cleft palate (Journal of Human Genetics, (2017), 62, 9, (861-863), 10.1038/jhg.2017.53)', Journal of Human Genetics, vol. 64, no. 7, pp. 701-702. https://doi.org/10.1038/s10038-019-0610-8

Kato K, Miya F, Hori I, Ieda D, Ohashi K, Negishi Y et al. Author Correction: A missense mutation in the HECT domain of NEDD4L identified in a girl with periventricular nodular heterotopia, polymicrogyria, and cleft palate (Journal of Human Genetics, (2017), 62, 9, (861-863), 10.1038/jhg.2017.53). Journal of Human Genetics. 2019 Jul 1;64(7):701-702. doi: 10.1038/s10038-019-0610-8

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title = "Author Correction: A missense mutation in the HECT domain of NEDD4L identified in a girl with periventricular nodular heterotopia, polymicrogyria, and cleft palate (Journal of Human Genetics, (2017), 62, 9, (861-863), 10.1038/jhg.2017.53)",

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 https://doi.org/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”.",

author = "Koji Kato and Fuyuki Miya and Ikumi Hori and Daisuke Ieda and Kei Ohashi and Yutaka Negishi and Ayako Hattori and Nobuhiko Okamoto and Mitsuhiro Kato and Tatsuhiko Tsunoda and Mami Yamasaki and Yonehiro Kanemura and Kenjiro Kosaki and Shinji Saitoh",

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T1 - Author Correction

T2 - A missense mutation in the HECT domain of NEDD4L identified in a girl with periventricular nodular heterotopia, polymicrogyria, and cleft palate (Journal of Human Genetics, (2017), 62, 9, (861-863), 10.1038/jhg.2017.53)

AU - Kato, Koji

AU - Miya, Fuyuki

AU - Hori, Ikumi

AU - Ieda, Daisuke

AU - Ohashi, Kei

AU - Negishi, Yutaka

AU - Hattori, Ayako

AU - Okamoto, Nobuhiko

AU - Kato, Mitsuhiro

AU - Tsunoda, Tatsuhiko

AU - Yamasaki, Mami

AU - Kanemura, Yonehiro

AU - Kosaki, Kenjiro

AU - Saitoh, Shinji

PY - 2019/7/1

Y1 - 2019/7/1

N2 - 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 https://doi.org/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”.

AB - 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 https://doi.org/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”.

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Author Correction: A missense mutation in the HECT domain of NEDD4L identified in a girl with periventricular nodular heterotopia, polymicrogyria, and cleft palate (Journal of Human Genetics, (2017), 62, 9, (861-863), 10.1038/jhg.2017.53)

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