Thymidine Kinase

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Domínguez-González, C., Madruga-Garrido, M., Hirano, M., Martí, I., Martín, M. A., Munell, F., Nascimento, A., Olivé, M., Quan, J., Sardina, M. D., Martí, R., & Paradas, C. (2021). Collaborative model for diagnosis and treatment of very rare diseases: experience in Spain with thymidine kinase 2 deficiency. Orphanet Journal of Rare Diseases, 16(1). https://doi.org/10.1186/s13023-021-02030-w
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