# Exome Sequencing Reveals Cubilin Mutation as a Single-Gene Cause of Proteinuria

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/exome-sequencing-reveals-cubilin-mutation-as-a-single-gene-cause-of-proteinuria/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Buğsu Övünç,Edgar A. Otto,Virginia Vega-Warner,Pawaree Saisawat,Shazia Ashraf,Gokul Ramaswami,Hanan Fathy,Dominik S. Schoeb,Gil Chernin,Robert H. Lyons,Engin Yılmaz,Friedhelm Hildebrandt |
| Citations | 113 |
| DOI | 10.1681/asn.2011040337 |
| Fields | Biochemistry, Genetics and Molecular Biology,Medicine |
| Open Access | true |
| OA Status | green |
| OA URL | http://hdl.handle.net/11655/16198 |
| OpenAlex ID | https://openalex.org/W1997733349 |
| PMID | 21903995 |
| Type | article |
| Year | 2011 |

## Paper authors

- [Dominik S. Schoeb](https://scholariq.org/researchers/dominik-s-schoeb/)
- [Gil Chernin](https://scholariq.org/researchers/gil-chernin/)

## Paper journal

- [Journal of the American Society of Nephrology](https://scholariq.org/journals/journal-of-the-american-society-of-nephrology/)

## Paper primary topic

- [Folate and B Vitamins Research](https://scholariq.org/topics/folate-and-b-vitamins-research/)

## Paper topics

- [Folate and B Vitamins Research](https://scholariq.org/topics/folate-and-b-vitamins-research/)
- [Renal Diseases and Glomerulopathies](https://scholariq.org/topics/renal-diseases-and-glomerulopathies/)
- [Porphyrin Metabolism and Disorders](https://scholariq.org/topics/porphyrin-metabolism-and-disorders/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.