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Page 1
Mitochondrial DNA depletion in sporadic inclusion body myositis.
Bhatt PS, Tzoulis C, Balafkan N, Miletic H, Tran GTT, Sanaker PS, Bindoff LA. Bhatt PS, et al. Among authors: balafkan n. Neuromuscul Disord. 2019 Mar;29(3):242-246. doi: 10.1016/j.nmd.2019.02.001. Epub 2019 Feb 10. Neuromuscul Disord. 2019. PMID: 30850168 Free article.
Molecular pathogenesis of polymerase γ-related neurodegeneration.
Tzoulis C, Tran GT, Coxhead J, Bertelsen B, Lilleng PK, Balafkan N, Payne B, Miletic H, Chinnery PF, Bindoff LA. Tzoulis C, et al. Among authors: balafkan n. Ann Neurol. 2014 Jul;76(1):66-81. doi: 10.1002/ana.24185. Epub 2014 Jun 14. Ann Neurol. 2014. PMID: 24841123 Free PMC article.
Disease-specific phenotypes in iPSC-derived neural stem cells with POLG mutations.
Liang KX, Kristiansen CK, Mostafavi S, Vatne GH, Zantingh GA, Kianian A, Tzoulis C, Høyland LE, Ziegler M, Perez RM, Furriol J, Zhang Z, Balafkan N, Hong Y, Siller R, Sullivan GJ, Bindoff LA. Liang KX, et al. Among authors: balafkan n. EMBO Mol Med. 2020 Oct 7;12(10):e12146. doi: 10.15252/emmm.202012146. Epub 2020 Aug 25. EMBO Mol Med. 2020. PMID: 32840960 Free PMC article.