Correction: Biallelic GALM pathogenic variants cause a novel type of galactosemia (Genetics in Medicine, (2019), 21, 6, (1286-1294), 10.1038/s41436-018-0340-x)

Yoichi Wada; Atsuo Kikuchi; Natsuko Arai-Ichinoi; Osamu Sakamoto; Yusuke Takezawa; Shinya Iwasawa; Tetsuya Niihori; Hiromi Nyuzuki; Yoko Nakajima; Erika Ogawa; Mika Ishige; Hiroki Hirai; Hideo Sasai; Ryoji Fujiki; Matsuyuki Shirota; Ryo Funayama; Masayuki Yamamoto; Tetsuya Ito; Osamu Ohara; Keiko Nakayama; Yoko Aoki; Seizo Koshiba; Toshiyuki Fukao; Shigeo Kure

doi:10.1038/s41436-020-0836-z

Correction: Biallelic GALM pathogenic variants cause a novel type of galactosemia (Genetics in Medicine, (2019), 21, 6, (1286-1294), 10.1038/s41436-018-0340-x)

Yoichi Wada, Atsuo Kikuchi, Natsuko Arai-Ichinoi, Osamu Sakamoto, Yusuke Takezawa, Shinya Iwasawa, Tetsuya Niihori, Hiromi Nyuzuki, Yoko Nakajima, Erika Ogawa, Mika Ishige, Hiroki Hirai, Hideo Sasai, Ryoji Fujiki, Matsuyuki Shirota, Ryo Funayama, Masayuki Yamamoto, Tetsuya Ito, Osamu Ohara, Keiko NakayamaYoko Aoki, Seizo Koshiba, Toshiyuki Fukao, Shigeo Kure

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

4 Citations (Scopus)

Abstract

In the original version of this Article the authors described a variant at the DNA level as “c.293delC.” This occurred several times in the Article as well as in the supplementary information. According to the HGVS-nomenclature recommendations (http://varnomen.hgvs.org/) it should be “c.294delC.” This has now been corrected in both the PDF and HTML versions of the Article and the supplementary information.

Original language	English
Pages (from-to)	1281
Number of pages	1
Journal	Genetics in Medicine
Volume	22
Issue number	7
DOIs	https://doi.org/10.1038/s41436-020-0836-z
Publication status	Published - 01-07-2020
Externally published	Yes

All Science Journal Classification (ASJC) codes

Genetics(clinical)

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10.1038/s41436-020-0836-z

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Wada, Y., Kikuchi, A., Arai-Ichinoi, N., Sakamoto, O., Takezawa, Y., Iwasawa, S., Niihori, T., Nyuzuki, H., Nakajima, Y., Ogawa, E., Ishige, M., Hirai, H., Sasai, H., Fujiki, R., Shirota, M., Funayama, R., Yamamoto, M., Ito, T., Ohara, O., ... Kure, S. (2020). Correction: Biallelic GALM pathogenic variants cause a novel type of galactosemia (Genetics in Medicine, (2019), 21, 6, (1286-1294), 10.1038/s41436-018-0340-x). Genetics in Medicine, 22(7), 1281. https://doi.org/10.1038/s41436-020-0836-z

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title = "Correction: Biallelic GALM pathogenic variants cause a novel type of galactosemia (Genetics in Medicine, (2019), 21, 6, (1286-1294), 10.1038/s41436-018-0340-x)",

abstract = "In the original version of this Article the authors described a variant at the DNA level as “c.293delC.” This occurred several times in the Article as well as in the supplementary information. According to the HGVS-nomenclature recommendations (http://varnomen.hgvs.org/) it should be “c.294delC.” This has now been corrected in both the PDF and HTML versions of the Article and the supplementary information.",

author = "Yoichi Wada and Atsuo Kikuchi and Natsuko Arai-Ichinoi and Osamu Sakamoto and Yusuke Takezawa and Shinya Iwasawa and Tetsuya Niihori and Hiromi Nyuzuki and Yoko Nakajima and Erika Ogawa and Mika Ishige and Hiroki Hirai and Hideo Sasai and Ryoji Fujiki and Matsuyuki Shirota and Ryo Funayama and Masayuki Yamamoto and Tetsuya Ito and Osamu Ohara and Keiko Nakayama and Yoko Aoki and Seizo Koshiba and Toshiyuki Fukao and Shigeo Kure",

note = "Publisher Copyright: {\textcopyright} 2020, American College of Medical Genetics and Genomics.",

year = "2020",

month = jul,

day = "1",

doi = "10.1038/s41436-020-0836-z",

language = "English",

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Wada, Y, Kikuchi, A, Arai-Ichinoi, N, Sakamoto, O, Takezawa, Y, Iwasawa, S, Niihori, T, Nyuzuki, H, Nakajima, Y, Ogawa, E, Ishige, M, Hirai, H, Sasai, H, Fujiki, R, Shirota, M, Funayama, R, Yamamoto, M, Ito, T, Ohara, O, Nakayama, K, Aoki, Y, Koshiba, S, Fukao, T & Kure, S 2020, 'Correction: Biallelic GALM pathogenic variants cause a novel type of galactosemia (Genetics in Medicine, (2019), 21, 6, (1286-1294), 10.1038/s41436-018-0340-x)', Genetics in Medicine, vol. 22, no. 7, pp. 1281. https://doi.org/10.1038/s41436-020-0836-z

TY - JOUR

T1 - Correction

T2 - Biallelic GALM pathogenic variants cause a novel type of galactosemia (Genetics in Medicine, (2019), 21, 6, (1286-1294), 10.1038/s41436-018-0340-x)

AU - Wada, Yoichi

AU - Kikuchi, Atsuo

AU - Arai-Ichinoi, Natsuko

AU - Sakamoto, Osamu

AU - Takezawa, Yusuke

AU - Iwasawa, Shinya

AU - Niihori, Tetsuya

AU - Nyuzuki, Hiromi

AU - Nakajima, Yoko

AU - Ogawa, Erika

AU - Ishige, Mika

AU - Hirai, Hiroki

AU - Sasai, Hideo

AU - Fujiki, Ryoji

AU - Shirota, Matsuyuki

AU - Funayama, Ryo

AU - Yamamoto, Masayuki

AU - Ito, Tetsuya

AU - Ohara, Osamu

AU - Nakayama, Keiko

AU - Aoki, Yoko

AU - Koshiba, Seizo

AU - Fukao, Toshiyuki

AU - Kure, Shigeo

PY - 2020/7/1

Y1 - 2020/7/1

N2 - In the original version of this Article the authors described a variant at the DNA level as “c.293delC.” This occurred several times in the Article as well as in the supplementary information. According to the HGVS-nomenclature recommendations (http://varnomen.hgvs.org/) it should be “c.294delC.” This has now been corrected in both the PDF and HTML versions of the Article and the supplementary information.

AB - In the original version of this Article the authors described a variant at the DNA level as “c.293delC.” This occurred several times in the Article as well as in the supplementary information. According to the HGVS-nomenclature recommendations (http://varnomen.hgvs.org/) it should be “c.294delC.” This has now been corrected in both the PDF and HTML versions of the Article and the supplementary information.

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U2 - 10.1038/s41436-020-0836-z

DO - 10.1038/s41436-020-0836-z

M3 - Comment/debate

C2 - 32499603

AN - SCOPUS:85085956157

SN - 1098-3600

VL - 22

SP - 1281

JO - Genetics in Medicine

JF - Genetics in Medicine

IS - 7

ER -

Correction: Biallelic GALM pathogenic variants cause a novel type of galactosemia (Genetics in Medicine, (2019), 21, 6, (1286-1294), 10.1038/s41436-018-0340-x)

Abstract

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