# Genetic heterogeneity of Barter's syndrome revealed by mutations in the K+ channel, ROMK

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/genetic-heterogeneity-of-barter-s-syndrome-revealed-by-mutations-in-the-k/

## Facts

| Field | Value |
| --- | --- |
| Author Names | David B. Simon,Fiona E. Karet,Juan Rodríguez‐Soriano,Jahed Hamdan,Antonio DiPietro,Howard Trachtman,Sami A. Sanjad,Richard P. Lifton |
| Citations | 827 |
| DOI | 10.1038/ng1096-152 |
| Fields | Biochemistry, Genetics and Molecular Biology,Medicine |
| Open Access | false |
| OA Status | closed |
| OpenAlex ID | https://openalex.org/W1995826486 |
| PMID | 8841184 |
| Type | article |
| Year | 1996 |

## Paper authors

- [Howard Trachtman](https://scholariq.org/researchers/howard-trachtman/)

## Paper primary topic

- [Ion Transport and Channel Regulation](https://scholariq.org/topics/ion-transport-and-channel-regulation/)

## Paper topics

- [Ion Transport and Channel Regulation](https://scholariq.org/topics/ion-transport-and-channel-regulation/)
- [Renal function and acid-base balance](https://scholariq.org/topics/renal-function-and-acid-base-balance/)
- [Ion channel regulation and function](https://scholariq.org/topics/ion-channel-regulation-and-function/)

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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.