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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1990 1
1995 1
2001 1
2002 1
2005 1
2008 1
2018 1
2019 1
2020 1
2021 2
2022 3
2024 0

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PubMed (OMIM) for id: 10935

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Page 1
Protein misfolding and clearance in the pathogenesis of a new infantile onset ataxia caused by mutations in PRDX3.
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. Martínez-Rubio D, et al. Hum Mol Genet. 2022 Nov 10;31(22):3897-3913. doi: 10.1093/hmg/ddac146. Hum Mol Genet. 2022. PMID: 35766882 Free PMC article.
Biallelic loss-of-function variations in PRDX3 cause cerebellar ataxia.
Rebelo AP, Eidhof I, Cintra VP, Guillot-Noel L, Pereira CV, Timmann D, Traschütz A, Schöls L, Coarelli G, Durr A, Anheim M, Tranchant C, van de Warrenburg B, Guissart C, Koenig M, Howell J, Moraes CT, Schenck A, Stevanin G, Züchner S, Synofzik M; PREPARE network. Rebelo AP, et al. Brain. 2021 Jun 22;144(5):1467-1481. doi: 10.1093/brain/awab071. Brain. 2021. PMID: 33889951
Punctiform and Polychromatic Pre-Descemet Corneal Dystrophy: Clinical Evaluation and Identification of the Genetic Basis.
Alió Del Barrio JL, Chung DD, Al-Shymali O, Barrington A, Jatavallabhula K, Swamy VS, Yébana P, Angélica Henríquez-Recine M, Boto-de-Los-Bueis A, Alió JL, Aldave AJ. Alió Del Barrio JL, et al. Am J Ophthalmol. 2020 Apr;212:88-97. doi: 10.1016/j.ajo.2019.11.024. Epub 2019 Nov 27. Am J Ophthalmol. 2020. PMID: 31782998 Free PMC article.
12 results