# Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/autosomal-dominant-hypophosphataemic-rickets-is-associated-with-mutations-in/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Kenneth E. White,W. Evans,Jeffery L.H. O'Riordan,Marcy C. Speer,Michael J. Econs,Bettina Lorenz‐Depiereux,Monika Grabowski,Thomas Meitinger,Tim M. Strom |
| Citations | 1,530 |
| DOI | 10.1038/81664 |
| Fields | Biochemistry, Genetics and Molecular Biology,Medicine |
| Open Access | false |
| OA Status | closed |
| OpenAlex ID | https://openalex.org/W1563425273 |
| PMID | 11062477 |
| Type | article |
| Year | 2000 |

## Paper authors

- [Thomas Meitinger](https://scholariq.org/researchers/thomas-meitinger/)
- [Michael J. Econs](https://scholariq.org/researchers/michael-j-econs/)
- [Tim M. Strom](https://scholariq.org/researchers/tim-m-strom/)

## Paper primary topic

- [Parathyroid Disorders and Treatments](https://scholariq.org/topics/parathyroid-disorders-and-treatments/)

## Paper topics

- [Parathyroid Disorders and Treatments](https://scholariq.org/topics/parathyroid-disorders-and-treatments/)
- [Fibroblast Growth Factor Research](https://scholariq.org/topics/fibroblast-growth-factor-research/)
- [Genetic Syndromes and Imprinting](https://scholariq.org/topics/genetic-syndromes-and-imprinting/)

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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.