Special Issue: DNA Helicases: Mechanisms, Biological Pathways, and Disease Relevance.

Genes (Basel) · 2021 · PMC8000711 · PMID 33804438

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highly significantno p-value reported

Given the importance of TWINKLE mutations for human diseases characterized by mitochondrial defects, neurodegeneration, and accelerated aging, the review by Peter and Falkenberg is a highly significant contribution to the field.

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