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bibliographicCitation Darin N, Siibak T, Peter B, Hedberg-Oldfors C, Kollberg G, Kalbin V, Moslemi AR, Macao B, Oldfors A, Falkenberg M. Functional analysis of a novel POLγA mutation associated with a severe perinatal mitochondrial encephalomyopathy. Neuromuscul Disord. 2021 Apr;31(4):348–58. doi: 10.1016/j.nmd.2021.01.004. PMID: 33579567.
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title Functional analysis of a novel POLγA mutation associated with a severe perinatal mitochondrial encephalomyopathy
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