Erratum: De novo variants in POLR3B cause ataxia, spasticity, and demyelinating neuropathy (The American Journal of Human Genetics (2021) 108(1) (186–193), (S0002929720304389), (10.1016/j.ajhg.2020.12.002))

Djurdja Djordjevic; Maxime Pinard; Marie Soleil Gauthier; Constance Smith-Hicks; Trevor L. Hoffman; Nicole I. Wolf; Renske Oegema; Ellen van Binsbergen; Berivan Baskin; Geneviève Bernard; Sébastien Fribourg; Benoit Coulombe; Grace Yoon

doi:10.1016/j.ajhg.2022.03.006

Erratum: De novo variants in POLR3B cause ataxia, spasticity, and demyelinating neuropathy (The American Journal of Human Genetics (2021) 108(1) (186–193), (S0002929720304389), (10.1016/j.ajhg.2020.12.002))

Djurdja Djordjevic, Maxime Pinard, Marie Soleil Gauthier, Constance Smith-Hicks, Trevor L. Hoffman, Nicole I. Wolf, Renske Oegema, Ellen van Binsbergen, Berivan Baskin, Geneviève Bernard, Sébastien Fribourg, Benoit Coulombe, Grace Yoon

Kennedy Krieger Institute

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

Abstract

(The American Journal of Human Genetics 108, 186–193; January 7, 2021) In the originally published version of this article, there is a typographical error for the variant c.3137G>A (p.Arg1046His) present in subject 3. This was inadvertently described as p.Arg1064His in Figures 2, 3, and S3, which appear corrected here and have been corrected in the online version of the article. The authors apologize for the error.

Original language	English (US)
Pages (from-to)	759-763
Number of pages	5
Journal	American journal of human genetics
Volume	109
Issue number	4
DOIs	https://doi.org/10.1016/j.ajhg.2022.03.006
State	Published - Apr 7 2022

ASJC Scopus subject areas

Genetics(clinical)
Genetics

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Djordjevic, D., Pinard, M., Gauthier, M. S., Smith-Hicks, C., Hoffman, T. L., Wolf, N. I., Oegema, R., van Binsbergen, E., Baskin, B., Bernard, G., Fribourg, S., Coulombe, B., & Yoon, G. (2022). Erratum: De novo variants in POLR3B cause ataxia, spasticity, and demyelinating neuropathy (The American Journal of Human Genetics (2021) 108(1) (186–193), (S0002929720304389), (10.1016/j.ajhg.2020.12.002)). American journal of human genetics, 109(4), 759-763. https://doi.org/10.1016/j.ajhg.2022.03.006

Erratum: De novo variants in POLR3B cause ataxia, spasticity, and demyelinating neuropathy (The American Journal of Human Genetics (2021) 108(1) (186–193), (S0002929720304389), (10.1016/j.ajhg.2020.12.002)). / Djordjevic, Djurdja; Pinard, Maxime; Gauthier, Marie Soleil et al.
In: American journal of human genetics, Vol. 109, No. 4, 07.04.2022, p. 759-763.

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

Djordjevic, D, Pinard, M, Gauthier, MS, Smith-Hicks, C, Hoffman, TL, Wolf, NI, Oegema, R, van Binsbergen, E, Baskin, B, Bernard, G, Fribourg, S, Coulombe, B & Yoon, G 2022, 'Erratum: De novo variants in POLR3B cause ataxia, spasticity, and demyelinating neuropathy (The American Journal of Human Genetics (2021) 108(1) (186–193), (S0002929720304389), (10.1016/j.ajhg.2020.12.002))', American journal of human genetics, vol. 109, no. 4, pp. 759-763. https://doi.org/10.1016/j.ajhg.2022.03.006

Djordjevic D, Pinard M, Gauthier MS, Smith-Hicks C, Hoffman TL, Wolf NI et al. Erratum: De novo variants in POLR3B cause ataxia, spasticity, and demyelinating neuropathy (The American Journal of Human Genetics (2021) 108(1) (186–193), (S0002929720304389), (10.1016/j.ajhg.2020.12.002)). American journal of human genetics. 2022 Apr 7;109(4):759-763. doi: 10.1016/j.ajhg.2022.03.006

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title = "Erratum: De novo variants in POLR3B cause ataxia, spasticity, and demyelinating neuropathy (The American Journal of Human Genetics (2021) 108(1) (186–193), (S0002929720304389), (10.1016/j.ajhg.2020.12.002))",

abstract = "(The American Journal of Human Genetics 108, 186–193; January 7, 2021) In the originally published version of this article, there is a typographical error for the variant c.3137G>A (p.Arg1046His) present in subject 3. This was inadvertently described as p.Arg1064His in Figures 2, 3, and S3, which appear corrected here and have been corrected in the online version of the article. The authors apologize for the error.",

author = "Djurdja Djordjevic and Maxime Pinard and Gauthier, {Marie Soleil} and Constance Smith-Hicks and Hoffman, {Trevor L.} and Wolf, {Nicole I.} and Renske Oegema and {van Binsbergen}, Ellen and Berivan Baskin and Genevi{\`e}ve Bernard and S{\'e}bastien Fribourg and Benoit Coulombe and Grace Yoon",

note = "Publisher Copyright: {\textcopyright} 2022 American Society of Human Genetics",

year = "2022",

month = apr,

day = "7",

doi = "10.1016/j.ajhg.2022.03.006",

language = "English (US)",

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AU - Djordjevic, Djurdja

AU - Pinard, Maxime

AU - Gauthier, Marie Soleil

AU - Smith-Hicks, Constance

AU - Hoffman, Trevor L.

AU - Wolf, Nicole I.

AU - Oegema, Renske

AU - van Binsbergen, Ellen

AU - Baskin, Berivan

AU - Bernard, Geneviève

AU - Fribourg, Sébastien

AU - Coulombe, Benoit

AU - Yoon, Grace

PY - 2022/4/7

Y1 - 2022/4/7

N2 - (The American Journal of Human Genetics 108, 186–193; January 7, 2021) In the originally published version of this article, there is a typographical error for the variant c.3137G>A (p.Arg1046His) present in subject 3. This was inadvertently described as p.Arg1064His in Figures 2, 3, and S3, which appear corrected here and have been corrected in the online version of the article. The authors apologize for the error.

AB - (The American Journal of Human Genetics 108, 186–193; January 7, 2021) In the originally published version of this article, there is a typographical error for the variant c.3137G>A (p.Arg1046His) present in subject 3. This was inadvertently described as p.Arg1064His in Figures 2, 3, and S3, which appear corrected here and have been corrected in the online version of the article. The authors apologize for the error.

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SN - 0002-9297

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SP - 759

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JO - American journal of human genetics

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Erratum: De novo variants in POLR3B cause ataxia, spasticity, and demyelinating neuropathy (The American Journal of Human Genetics (2021) 108(1) (186–193), (S0002929720304389), (10.1016/j.ajhg.2020.12.002))

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