Cargando…
312 Homozygous G2 APOL1 Allele and a Heterozygous Complement 5 Variant in Hypertensive Chronic Kidney Disease
Formato: | Online Artículo Texto |
---|---|
Lenguaje: | English |
Publicado: |
Published by Elsevier Inc.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7973198/ http://dx.doi.org/10.1053/j.ajkd.2021.02.317 |
Ejemplares similares
-
APOL1 genetic variants, chronic kidney diseases and hypertension in mixed ancestry South Africans
por: Matsha, Tandi E, et al.
Publicado: (2015) -
311 Acute Kidney Injury and Collapsing Glomerulopathy in Patient With COVID-19 and Homozygous for APOL1 Gene Variant
Publicado: (2021) -
G1 is the major APOL1 risk allele for hypertension-attributed nephropathy in Central Africa
por: Sumaili, Ernest K, et al.
Publicado: (2018) -
Should kidney donors be genotyped for APOL1 risk alleles?
por: Freedman, Barry I., et al.
Publicado: (2015) -
313 Homozygous High-Risk APOL1 Variant and Heterozygous COL4A4 Mutation in an African American Patient With Collapsing Focal Segmental Glomerulonephritis
Publicado: (2021)