The evolving story of apolipoprotein L1 nephropathy: the end of the beginning

Genetic coding variants in APOL1, which encodes apolipoprotein L1 (APOL1), were identified in 2010 and are relatively common among individuals of sub-Saharan African ancestry. Approximately 13% of African Americans carry two APOL1 risk alleles. These variants, termed G1 and G2, are a frequent cause...

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Detalles Bibliográficos
Autores principales: Daneshpajouhnejad, Parnaz, Kopp, Jeffrey B., Winkler, Cheryl A., Rosenberg, Avi Z.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8877744/
https://www.ncbi.nlm.nih.gov/pubmed/35217848
http://dx.doi.org/10.1038/s41581-022-00538-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8877744/
https://www.ncbi.nlm.nih.gov/pubmed/35217848
http://dx.doi.org/10.1038/s41581-022-00538-3

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