A novel rare CUBN variant and three additional genes identified in Europeans with and without diabetes: results from an exome-wide association study of albuminuria
International audience AIMS/HYPOTHESIS: Identifying rare coding variants associated with albuminuria may open new avenues for preventing chronic kidney disease and end-stage renal disease, which are highly prevalent in individuals with diabetes. Efforts to identify genetic susceptibility variants fo...
Published in: | Diabetologia |
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Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Other Authors: | , , , , , , , , , , , , , , , , , , , , , , , , |
Format: | Article in Journal/Newspaper |
Language: | English |
Published: |
HAL CCSD
2019
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Subjects: | |
Online Access: | https://hal.sorbonne-universite.fr/hal-01976819 https://hal.sorbonne-universite.fr/hal-01976819/document https://hal.sorbonne-universite.fr/hal-01976819/file/Ahluwalia2019_Article_ANovelRareCUBNVariantAndThreeA.pdf https://doi.org/10.1007/s00125-018-4783-z |