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

医学部臨床遺伝学センター

研究成果: Comment/debate › 査読

抄録

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”.

本文言語	English
ページ（範囲）	701-702
ページ数	2
ジャーナル	Journal of Human Genetics
巻	64
号	7
DOI	https://doi.org/10.1038/s10038-019-0610-8
出版ステータス	Published - 2019 7月 1

ASJC Scopus subject areas

遺伝学
遺伝学（臨床）

文献へのアクセス

10.1038/s10038-019-0610-8

他のファイルとリンク

フィンガープリント

「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)」の研究トピックを掘り下げます。これらがまとまってユニークなフィンガープリントを構成します。

引用スタイル

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 その他.
In: Journal of Human Genetics, Vol. 64, No. 7, 01.07.2019, p. 701-702.

研究成果: Comment/debate › 査読

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 その他. 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 7月 1;64(7):701-702. doi: 10.1038/s10038-019-0610-8

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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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AU - Kato, Koji

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AU - Ieda, Daisuke

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AU - Okamoto, Nobuhiko

AU - Kato, Mitsuhiro

AU - Tsunoda, Tatsuhiko

AU - Yamasaki, Mami

AU - Kanemura, Yonehiro

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AU - Saitoh, Shinji

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