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    المساهمون: Constantinou-Deltas, Constantinos D. [0000-0001-5549-9169]

    المصدر: PLoS ONE
    PLoS ONE, Vol 8, Iss 3, p e57925 (2013)

    مصطلحات موضوعية: Male, Pathology, genetic association, kidney disease, genetic risk, urologic and male genital diseases, Gastroenterology, Linkage Disequilibrium, lcsh:Science, quantitative analysis, adult, thin basement membrane nephropathy, Molecular Motor Proteins, allele, Apolipoprotein L1, Proteinuria, real time polymerase chain reaction, Nephrology, Cohort, Disease Progression, Medicine, disease severity, Lipoproteins, HDL, marker gene, medicine.medical_specialty, phenotype, Single-nucleotide polymorphism, glomerulopathy, Nephropathy, complement component C3, Molecular Genetics, Genetic Mutation, Genetics, Humans, human, Renal Insufficiency, Chronic, genetic epistasis, Biology, COL4A3 gene, Alleles, Aged, Hematuria, Myosin Heavy Chains, lcsh:R, medicine.disease, major clinical study, gene linkage disequilibrium, gene function, Apolipoproteins, lcsh:Q, Dialysis, haplotype, lcsh:Medicine, Epigenesis, Genetic, hereditary hematuria, APOL1 gene, single nucleotide polymorphism, genetic variability, Molecular Cell Biology, Chronic Kidney Disease, gene mutation, Multidisciplinary, messenger RNA, article, COL4A4 gene, Exons, Middle Aged, biological marker, female, CFHR5 gene, Female, Research Article, Clinical Pathology, sex difference, Polymorphism, Single Nucleotide, male, Glomerulopathy, Diagnostic Medicine, Internal medicine, medicine, controlled study, complement component C3 gene, Alport syndrome, Genetic Association Studies, Clinical Genetics, business.industry, Mutation Types, Human Genetics, gene structure, myosin heavy chain 9 gene, hematuria, Haplotypes, Genetics of Disease, CFHR5 nephropathy, business, CFHR5, Kidney disease