Protein misfolding and clearance in the pathogenesis of a new infantile onset ataxia caused by mutations in PRDX3.

MLA

Martínez-Rubio, Dolores, et al. “Protein Misfolding and Clearance in the Pathogenesis of a New Infantile Onset Ataxia Caused by Mutations in PRDX3.” Human Molecular Genetics, vol. 31, no. 22, Nov. 2022, pp. 3897–913. EBSCOhost, https://doi.org/10.1093/hmg/ddac146.

APA

Martínez-Rubio, D., Rodríguez-Prieto, Á., Sancho, P., Navarro-González, C., Gorría-Redondo, N., Miquel-Leal, J., Marco-Marín, C., Jenkins, A., Soriano-Navarro, M., Hernández, A., Pérez-Dueñas, B., Fazzari, P., Aguilera-Albesa, S., & Espinós, C. (2022). Protein misfolding and clearance in the pathogenesis of a new infantile onset ataxia caused by mutations in PRDX3. Human Molecular Genetics, 31(22), 3897–3913. https://doi.org/10.1093/hmg/ddac146

Chicago

Martínez-Rubio, Dolores, Ángela Rodríguez-Prieto, Paula Sancho, Carmen Navarro-González, Nerea Gorría-Redondo, Javier Miquel-Leal, Clara Marco-Marín, et al. 2022. “Protein Misfolding and Clearance in the Pathogenesis of a New Infantile Onset Ataxia Caused by Mutations in PRDX3.” Human Molecular Genetics 31 (22): 3897–3913. doi:10.1093/hmg/ddac146.