Article

CUBN Gene Mutations May Cause Focal Segmental Glomerulosclerosis (FSGS) in Children

2021-09-03

Abstract excerpt

<h4>Background: </h4> CUBN gene mutation is extremely rare and thought to only presented as tubular proteinuria without glomerular involvement. Here, we present 3 patients with prominent proteinuria and FSGS in renal pathologies caused by novel CUBN gene mutations. <h4>Method: </h4> Whole exome sequencing was performed in three children. CUBN gene mutations were found and then verified by sanger sequencing. Their...

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Literature Corpus work: f32e52fb-cd5b-5ec4-ba77-e76b87fab5d2
DOI: 10.21203/rs.3.rs-753923/v1

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