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2. Pelayo, Gonçalo, Paiva Coelho, Margarida, Correia, Joana, Vilarinho, Laura, Martins, Esmeralda. 2024. Phenotyping mitochondrial glutamyl-tRNA synthetase deficiency (EARS2): A case series and systematic literature review. In Neurobiology of disease, 200, 106644. doi:10.1016/j.nbd.2024.106644. https://pubmed.ncbi.nlm.nih.gov/39173847/
3. Barbosa-Gouveia, Sofia, González-Vioque, Emiliano, Hermida, Álvaro, Rodenburg, Richard, Couce, María-Luz. 2020. Identification of a Novel Variant in EARS2 Associated with a Severe Clinical Phenotype Expands the Clinical Spectrum of LTBL. In Genes, 11, . doi:10.3390/genes11091028. https://pubmed.ncbi.nlm.nih.gov/32887222/
4. Wang, Ling, Deng, Xuemei, Tang, Jiaxi, Liao, Yong, Li, Yongsheng. 2025. Identification of EARS2 as a Potential Biomarker with Diagnostic, Prognostic, and Therapeutic Implications in Colorectal Cancer. In ImmunoTargets and therapy, 14, 65-85. doi:10.2147/ITT.S499680. https://pubmed.ncbi.nlm.nih.gov/39906030/
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7. Taskin, Birce Dilge, Karalok, Zeynep Selen, Gurkas, Esra, Yilmaz, Cahide, Pearl, Phillip Lawrence. 2016. Early-Onset Mild Type Leukoencephalopathy Caused by a Homozygous EARS2 Mutation. In Journal of child neurology, 31, 938-41. doi:10.1177/0883073816630087. https://pubmed.ncbi.nlm.nih.gov/26893310/
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