1. Lata, Elisabeth, Choquet, Karine, Sagliocco, Francis, Bernard, Geneviève, Teichmann, Martin. 2021. RNA Polymerase III Subunit Mutations in Genetic Diseases. In Frontiers in molecular biosciences, 8, 696438. doi:10.3389/fmolb.2021.696438. https://pubmed.ncbi.nlm.nih.gov/34395528/
2. Li, Yi-Fei, Hou, Qiong-Qiong, Zhao, Shuang, Tang, Min, Li, Lin. 2022. Identification of tumor-specific neoantigens and immune clusters of hepatocellular carcinoma for mRNA vaccine development. In Journal of cancer research and clinical oncology, 149, 623-637. doi:10.1007/s00432-022-04285-7. https://pubmed.ncbi.nlm.nih.gov/36239794/
3. Saadat, Ali, Gouttenoire, Jérôme, Ripellino, Paolo, Fellay, Jacques, Fraga, Montserrat. 2023. Inborn errors of type I interferon immunity in patients with symptomatic acute hepatitis E. In Hepatology (Baltimore, Md.), 79, 1421-1431. doi:10.1097/HEP.0000000000000701. https://pubmed.ncbi.nlm.nih.gov/38079352/
4. Ogunjimi, Benson, Zhang, Shen-Ying, Sørensen, Katrine B, Paludan, Søren R, Mogensen, Trine H. 2017. Inborn errors in RNA polymerase III underlie severe varicella zoster virus infections. In The Journal of clinical investigation, 127, 3543-3556. doi:10.1172/JCI92280. https://pubmed.ncbi.nlm.nih.gov/28783042/
5. Saul, Michael C, Stevenson, Sharon A, Zhao, Changjiu, Eisinger, Brian E, Gammie, Stephen C. 2018. Genomic variants in an inbred mouse model predict mania-like behaviors. In PloS one, 13, e0197624. doi:10.1371/journal.pone.0197624. https://pubmed.ncbi.nlm.nih.gov/29768498/
6. Harich, Benjamin, van der Voet, Monique, Klein, Marieke, Schenck, Annette, Franke, Barbara. 2020. From Rare Copy Number Variants to Biological Processes in ADHD. In The American journal of psychiatry, 177, 855-866. doi:10.1176/appi.ajp.2020.19090923. https://pubmed.ncbi.nlm.nih.gov/32600152/
7. Codina-Solà, Marta, Rodríguez-Santiago, Benjamín, Homs, Aïda, Pérez-Jurado, Luis Alberto, Cuscó, Ivon. 2015. Integrated analysis of whole-exome sequencing and transcriptome profiling in males with autism spectrum disorders. In Molecular autism, 6, 21. doi:10.1186/s13229-015-0017-0. https://pubmed.ncbi.nlm.nih.gov/25969726/
8. Ceylan, A C, Sahin, I, Erdem, H B, Boduroglu, K, Alikasifoglu, M. 2019. An eight-case 1q21 region series: novel aberrations and clinical variability with new features. In Journal of intellectual disability research : JIDR, 63, 548-557. doi:10.1111/jir.12592. https://pubmed.ncbi.nlm.nih.gov/30773728/
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