Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 4 (of 4 Records) |
Query Trace: Alpers Syndrome[original query] |
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Variations of mitochondrial DNA polymerase ? in patients with Parkinson's disease. Journal of neurology 2013 Dec 260 (12): 3144-9. Ylönen S, Ylikotila P, Siitonen A, Finnilä S, Autere J, Majamaa |
The presence of anaemia negatively influences survival in patients with POLG disease. Journal of inherited metabolic disease 2017 9 40 (6): 861-866. Hikmat Omar, Tzoulis Charalampos, Klingenberg Claus, Rasmussen Magnhild, Tallaksen Chantal M E, Brodtkorb Eylert, Fiskerstrand Torunn, McFarland Robert, Rahman Shamima, Bindoff Laurence |
Astrocytic pathology in Alpers' syndrome. Acta neuropathologica communications 2023 5 11 (1): 86. Laura A Smith, Chun Chen, Nichola Z Lax, Robert W Taylor, Daniel Erskine, Robert McFarla |
The Y831C Mutation of the POLG Gene in Dementia. Biomedicines 2023 5 11 (4): . Eugenia Borgione, Mariangela Lo Giudice, Sandro Santa Paola, Marika Giuliano, Giuseppe Lanza, Mariagiovanna Cantone, Raffaele Ferri, Carmela Scude |
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