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• W3092854987 abstract "DNA replication is fundamental for cell proliferation in all organisms. Nonetheless, components of the replisome have been implicated in human disease, and here we report PRIM1 encoding the catalytic subunit of DNA primase as a novel disease gene. Using a variant classification agnostic approach, biallelic mutations in PRIM1 were identified in five individuals. PRIM1 protein levels were markedly reduced in patient cells, accompanied by replication fork asymmetry, increased interorigin distances, replication stress, and prolonged S-phase duration. Consequently, cell proliferation was markedly impaired, explaining the patients’ extreme growth failure. Notably, phenotypic features distinct from those previously reported with DNA polymerase genes were evident, highlighting differing developmental requirements for this core replisome component that warrant future investigation." @default.
• W3092854987 created "2020-10-22" @default.
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• W3092854987 date "2020-10-15" @default.
• W3092854987 modified "2023-10-15" @default.
• W3092854987 title "PRIM1 deficiency causes a distinctive primordial dwarfism syndrome" @default.
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• W3092854987 doi "https://doi.org/10.1101/gad.340190.120" @default.
• W3092854987 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/7608753" @default.
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• W3092854987 hasPublicationYear "2020" @default.
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