Missense mutations in the APOL1 gene are highly associated with end stage kidney disease risk previously attributed to the MYH9 gene. [electronic resource]
Producer: 20100907Description: 345-50 p. digitalISSN:- 1432-1203
- Africa
- Apolipoprotein L1
- Apolipoproteins -- genetics
- Chromosome Mapping
- Genetic Predisposition to Disease
- Haplotypes
- Humans
- Kidney Failure, Chronic -- genetics
- Linkage Disequilibrium
- Lipoproteins, HDL -- genetics
- Molecular Motor Proteins -- genetics
- Mutation, Missense
- Myosin Heavy Chains -- genetics
- Phenotype
- Polymorphism, Single Nucleotide
- Risk Factors
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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