Article

Exome wide association study on Albuminuria identifies a novel rare variant in <i>CUBN</i> and additional genes, in 33985 Europeans with and without diabetes

2018-06-27

Abstract excerpt

Identifying rare coding variants associated with albuminuria may open new avenues for preventing chronic kidney disease (CKD) and end-stage renal disease which are highly prevalent in patients with diabetes. Efforts to identify genetic susceptibility variants for albuminuria have so far been limited with the majority of studies focusing on common variants. We performed an exome-wide association study to identify c...

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Literature Corpus work: cead0bf8-f25b-50b0-883a-a3e5fee9ea38
DOI: 10.1101/355990

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