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Michele Salemi, Giuseppe Lanza, Maria Grazia Salluzzo, Francesca A. Schillaci, Francesco Domenico Di Blasi, Angela Cordella, Salvatore Caniglia, Bartolo Lanuzza, Manuela Morreale, Pietro Marano, Mariangela Tripodi & Raffaele Ferri. (2023) A Next-Generation Sequencing Study in a Cohort of Sicilian Patients with Parkinson’s Disease. Biomedicines 11:12, pages 3118.
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Marta Giannini & Odil Porrua. (2023) Senataxin: A key actor in RNA metabolism, genome integrity and neurodegeneration. Biochimie.
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Sina Shadfar, Sonam Parakh, Md Shafi Jamali & Julie D. Atkin. (2023) Redox dysregulation as a driver for DNA damage and its relationship to neurodegenerative diseases. Translational Neurodegeneration 12:1.
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Rupesh Kumar, Zubbair Malik, Manisha Singh, R. Rachana, Shalini Mani, Kalaiarasan Ponnusamy & Shazia Haider. (2023) Amyotrophic Lateral Sclerosis Risk Genes and Suppressor. Current Gene Therapy 23:2, pages 148-162.
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Maia Farrugia Wismayer, Andrew Farrugia Wismayer, Rebecca Borg, Karl Bonavia, André Abela, Charmaine Chircop, Josanne Aquilina, Doriette Soler, Adrian Pace, Malcolm Vella, Neville Vassallo & Ruben J. Cauchi. (2023) Genetic landscape of ALS in Malta based on a quinquennial analysis. Neurobiology of Aging 123, pages 200-207.
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Anni Zhang, Hongbei Xu, Jing Huang, Huilan Gong, Shipeng Guo, Xiaoyang Lei & Dian He. (2022) Coexisting amyotrophic lateral sclerosis and chorea: A case report and literature review. Medicine 101:52, pages e32452.
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André Brannvoll, Xiaoyu Xue, Youngho Kwon, Smaragdi Kompocholi, Anne Katrine W. Simonsen, Keerthana S. Viswalingam, Leticia Gonzalez, Ian D. Hickson, Vibe H. Oestergaard, Hocine W. Mankouri, Patrick Sung & Michael Lisby. (2020) The ZGRF1 Helicase Promotes Recombinational Repair of Replication-Blocking DNA Damage in Human Cells. Cell Reports 32:1, pages 107849.
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Viviana Pensato, Stefania Magri, Eleonora Dalla Bella, Pierpaola Tannorella, Enrica Bersano, Gianni Sorarù, Marta Gatti, Nicola Ticozzi, Franco Taroni, Giuseppe Lauria, Caterina Mariotti & Cinzia Gellera. (2020) Sorting Rare ALS Genetic Variants by Targeted Re-Sequencing Panel in Italian Patients: OPTN, VCP, and SQSTM1 Variants Account for 3% of Rare Genetic Forms. Journal of Clinical Medicine 9:2, pages 412.
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