article · New England Journal of Medicine
The abstract on record is too brief for a reliable plain-language summary, so none has been generated.
In this study, monoallelic <i>APOL1</i> variants were associated with 18% higher odds of CKD and 61% higher odds of focal segmental glomerulosclerosis; biallelic <i>APOL1</i> variants were associated with 25% higher odds of CKD and 84% higher odds of focal segmental glomerulosclerosis. (Funded by the National Human Genome Research Institute and others.).
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DOI: 10.1056/nejmoa2404211
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