Power and Pitfalls of Computational Methods to Identify New Genes Responsible for Acute Liver Failure of Indeterminate Etiology in Adults
- PMID: 32955204
- PMCID: PMC7447419
- DOI: 10.14309/ctg.0000000000000180
Power and Pitfalls of Computational Methods to Identify New Genes Responsible for Acute Liver Failure of Indeterminate Etiology in Adults
Erratum in
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Correction to: Power and Pitfalls of Computational Methods to Identify New Genes Responsible for Acute Liver Failure of Indeterminate Etiology in Adults.Clin Transl Gastroenterol. 2020 Sep;11(9):e00248. doi: 10.14309/ctg.0000000000000248. Clin Transl Gastroenterol. 2020. PMID: 33094952 Free PMC article. No abstract available.
Conflict of interest statement
Comment in
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Whole Exome Sequencing Among 26 Patients With Indeterminate Acute Liver Failure: Response to Letter to the Editor.Clin Transl Gastroenterol. 2020 Aug;11(8):e00187. doi: 10.14309/ctg.0000000000000187. Clin Transl Gastroenterol. 2020. PMID: 32955205 Free PMC article. No abstract available.
Comment on
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Whole Exome Sequencing Among 26 Patients With Indeterminate Acute Liver Failure: A Pilot Study.Clin Transl Gastroenterol. 2019 Oct;10(10):e00087. doi: 10.14309/ctg.0000000000000087. Clin Transl Gastroenterol. 2019. PMID: 31609742 Free PMC article.
References
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- Karczewski KJ, Francioli LC, Tiao G, et al. Variation across 141,456 human exomes and genomes reveals the spectrum of loss-of-function intolerance across human protein-coding genes. bioRxiv 2019:531210.
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