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Ancestral β-globin gene haplotypes modify β-thalassemia severity in a mouse model [bone marrow, spleen]

GSE260901 Mus musculus Expression profiling by high throughput sequencing 40 samples 2024/12/18 GPL24247
Summary
β-Thalassemia is a prevalent anemia caused by mutations in the HBB (β-globin) gene. We show that the severity of β-thalassemia in the frequently studied Hbbth3/+ mouse model is influenced by ancestral β-globin gene (Hbb) haplotypes that differ in common strains.
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NCBI GEO page ↗ Paper (PMID 38536944) ↗ {# Names what the click gives you. "Open in finder" meant nothing to a visitor who arrived from a search engine and has never seen the tool. #} Find more mouse RNA-seq datasets →
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