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Comment
. 2021 Mar;23(3):587-588.
doi: 10.1038/s41436-020-01013-9. Epub 2020 Oct 22.

Correspondence on "Aminoacyl-tRNA synthetase deficiencies in search of common themes" by Fuchs et al

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Free article
Comment

Correspondence on "Aminoacyl-tRNA synthetase deficiencies in search of common themes" by Fuchs et al

Yan-Wen Shen et al. Genet Med. 2021 Mar.
Free article

Erratum in

No abstract available

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Comment in

  • Response to Shen and Zou.
    Kok G, van Karnebeek CDM, Fuchs SA. Kok G, et al. Genet Med. 2021 Mar;23(3):589-590. doi: 10.1038/s41436-020-01014-8. Epub 2020 Oct 22. Genet Med. 2021. PMID: 33087890 No abstract available.

Comment on

  • Aminoacyl-tRNA synthetase deficiencies in search of common themes.
    Fuchs SA, Schene IF, Kok G, Jansen JM, Nikkels PGJ, van Gassen KLI, Terheggen-Lagro SWJ, van der Crabben SN, Hoeks SE, Niers LEM, Wolf NI, de Vries MC, Koolen DA, Houwen RHJ, Mulder MF, van Hasselt PM. Fuchs SA, et al. Genet Med. 2019 Feb;21(2):319-330. doi: 10.1038/s41436-018-0048-y. Epub 2018 Jun 6. Genet Med. 2019. PMID: 29875423 Free PMC article.

References

    1. Fuchs SA, Schene IF, Kok G, et al. Aminoacyl-tRNA synthetase deficiencies in search of common themes. Genet Med. 2019;21:319–330. - DOI
    1. Fuchs SA, Schene IF, Kok G, et al. Correction: Aminoacyl-tRNA synthetase deficiencies in search of common themes. Genet Med. 2020. https://doi.org/10.1038/s41436-020-00966-1 [Epub ahead of print].
    1. National Center for Biotechnology Information. GenBank database. https://www.ncbi.nlm.nih.gov/protein/AAA98797.1/ . Accessed 3 May 1996.
    1. Johannesen KM, Mitter D, Janowski R, et al. Defining and expanding the phenotype of QARS-associated developmental epileptic encephalopathy. Neurol Genet. 2019;5:e373. - DOI
    1. Shen YW, Weng ZF, He W, et al. [QARS1 gene related glutaminyl-tRNA synthetase deficiency syndrome: report of three cases and a review of literature]. Zhonghua Er Ke Za Zhi. 2020;58:1006–1012. Chinese. https://doi.org/10.3760/cma.j.cn112140-20200603-00571 .

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