Correspondence on "Aminoacyl-tRNA synthetase deficiencies in search of common themes" by Fuchs et al
- PMID: 33087889
- DOI: 10.1038/s41436-020-01013-9
Correspondence on "Aminoacyl-tRNA synthetase deficiencies in search of common themes" by Fuchs et al
Erratum in
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Correction to: Correspondence on "AminoacyltRNA synthetase deficiencies in search of common themes" by Fuchs et al.Genet Med. 2021 Nov;23(11):2231. doi: 10.1038/s41436-021-01160-7. Genet Med. 2021. PMID: 33879871 No abstract available.
Comment in
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Response to Shen and Zou.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
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Aminoacyl-tRNA synthetase deficiencies in search of common themes.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
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- Fuchs SA, Schene IF, Kok G, et al. Aminoacyl-tRNA synthetase deficiencies in search of common themes. Genet Med. 2019;21:319–330. - DOI
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- 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].
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- National Center for Biotechnology Information. GenBank database. https://www.ncbi.nlm.nih.gov/protein/AAA98797.1/ . Accessed 3 May 1996.
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- 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
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- 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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