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Increase in DNA methylation in patients with amyotrophic lateral sclerosis carriers of not fully penetrant SOD1 mutations.
Coppedè F, Stoccoro A, Mosca L, Gallo R, Tarlarini C, Lunetta C, Marocchi A, Migliore L, Penco S. Coppedè F, et al. Among authors: tarlarini c. Amyotroph Lateral Scler Frontotemporal Degener. 2018 Feb;19(1-2):93-101. doi: 10.1080/21678421.2017.1367401. Epub 2017 Sep 1. Amyotroph Lateral Scler Frontotemporal Degener. 2018. PMID: 28859526
Wide phenotypic spectrum of the TARDBP gene: homozygosity of A382T mutation in a patient presenting with amyotrophic lateral sclerosis, Parkinson's disease, and frontotemporal lobar degeneration, and in neurologically healthy subject.
Mosca L, Lunetta C, Tarlarini C, Avemaria F, Maestri E, Melazzini M, Corbo M, Penco S. Mosca L, et al. Among authors: tarlarini c. Neurobiol Aging. 2012 Aug;33(8):1846.e1-4. doi: 10.1016/j.neurobiolaging.2012.01.108. Epub 2012 Mar 6. Neurobiol Aging. 2012. PMID: 22398199
28 results