# INF2 mutations cause kidney disease through a gain-of-function mechanism

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/inf2-mutations-cause-kidney-disease-through-a-gain-of-function-mechanism/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Balajikarthick Subramanian,Sarah Williams,Sophie Karp,Marie-Flore Hennino,Sonako Jacas,Miriam Lee,Cristian V. Riella,Seth L. Alper,Henry N. Higgs,Martin R. Pollak |
| Citations | 15 |
| DOI | 10.1126/sciadv.adr1017 |
| Fields | Biochemistry, Genetics and Molecular Biology,Medicine |
| Open Access | true |
| OA Status | gold |
| OA URL | https://doi.org/10.1126/sciadv.adr1017 |
| OpenAlex ID | https://openalex.org/W4404307330 |
| PMID | 39536114 |
| Type | article |
| Year | 2024 |

## Paper authors

- [Cristian V. Riella](https://scholariq.org/researchers/cristian-v-riella/)

## Paper primary topic

- [Renal Diseases and Glomerulopathies](https://scholariq.org/topics/renal-diseases-and-glomerulopathies/)

## Paper topics

- [Renal Diseases and Glomerulopathies](https://scholariq.org/topics/renal-diseases-and-glomerulopathies/)
- [Renal and related cancers](https://scholariq.org/topics/renal-and-related-cancers/)
- [Chronic Kidney Disease and Diabetes](https://scholariq.org/topics/chronic-kidney-disease-and-diabetes/)

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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.