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Literature Workspace

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References
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1 reference

Research article 2019 Reviewed MVA Hackathon 2026 — BUB1B

BubR1 allelic effects drive phenotypic heterogeneity in mosaic-variegated aneuploidy progeria syndrome

Cynthia J. Sieben, Karthik B. Jeganathan, Grace G. Nelson and 8 more Journal of Clinical Investigation

Mosaic-variegated aneuploidy (MVA) syndrome is a rare childhood disorder characterized by biallelic BUBR1, CEP57, or TRIP13 aberrations; increased chromosome missegregation; and a broad spectrum of clinical features, inc… abstract via OpenAlex

Evidence snapshot note: Sieben et al. — allelic effects in MVA progeria syndrome. Model: Mouse BubR1 L1002P ortholog model of human L1012P with hypomorphic or truncating alleles. Where: Abstract and Figures 1-3; related variant, not N1002K · cited by MVA-N1002K-GATE-002

  • Aging
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  • Cellular senescence
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