The APOL1 p.N264K variant is co-inherited with the G2 kidney disease risk variant through a proximity recombination event

Simeone, C. A., McNulty, M. T., Gupta, Y., Genovese, G., Sampson, M. G., Sanna-Cherchi, S., Friedman, D. J., & Pollak, M. R. (2024). The APOL1 p.N264K variant is co-inherited with the G2 kidney disease risk variant through a proximity recombination event. G3: Genes, Genomes, Genetics. https://doi.org/10.1093/g3journal/jkae290
Authors:
Christopher A. Simeone
Michelle Mcnulty
Yask Gupta
Giulio Genovese
Matthew G. Sampson
Simone Sanna‐Cherchi
David J. Friedman
Martin R. Pollak
Affiliated Authors:
Yask Gupta
Simone Sanna‐Cherchi
Columbia Affiliation:
Subjects:
Apolipoprotein L1 (MeSH)
Genetic Predisposition to Disease (MeSH)
Recombination, Genetic (MeSH)
Kidney Diseases (MeSH)
Polymorphism, Single Nucleotide (MeSH)
Haplotypes (MeSH)
Lipoproteins, HDL (MeSH)
Apolipoproteins (MeSH)
Pathophysiology of Glomerular Diseases and Nephrotic Syndromes (OpenAlex Topic)
Genomic Aberrations and Treatment of Chronic Lymphocytic Leukemia (OpenAlex Topic)
Author Keywords:
haplotype
apol1
recombination
kidney disease
elink
Publication Type:
Article
Unique ID:
10.1093/g3journal/jkae290
PMID:
39658338
DOI:
10.1093/g3journal/jkae290
Journal:
G3: Genes, Genomes, Genetics
Publication Date:
Data Source:
OpenAlex
Source Link:
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