UBD modifies APOL1-induced kidney disease risk
People of recent African ancestry develop kidney disease at much higher rates than most other groups. Two specific coding variants in the Apolipoprotein-L1 gene APOL1 termed G1 and G2 are the causal drivers of much of this difference in risk, following a recessive pattern of inheritance. However, mo...
Saved in:
Published in | Proceedings of the National Academy of Sciences - PNAS Vol. 115; no. 13; pp. 3446 - 3451 |
---|---|
Main Authors | , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
National Academy of Sciences
27.03.2018
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Be the first to leave a comment!