# Mutations in LPIN1 Cause Recurrent Acute Myoglobinuria in Childhood

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/mutations-in-lpin1-cause-recurrent-acute-myoglobinuria-in-childhood/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Avraham Zeharia,Avraham Shaag,Riekelt H. Houtkooper,Tareq Hindi,Pascale de Lonlay,Gilli Erez,Laurence Hubert,Ann Saada,Yves de Keyzer,Gideon Eshel,Frédéric M. Vaz,Ophry Pines,Orly Elpeleg |
| Citations | 221 |
| DOI | 10.1016/j.ajhg.2008.09.002 |
| Fields | Biochemistry, Genetics and Molecular Biology,Medicine |
| Open Access | true |
| OA Status | bronze |
| OA URL | http://www.cell.com/article/S0002929708004898/pdf |
| OpenAlex ID | https://openalex.org/W1989595226 |
| PMID | 18817903 |
| Type | article |
| Year | 2008 |

## Paper authors

- [Orly Elpeleg](https://scholariq.org/researchers/orly-elpeleg/)

## Paper primary topic

- [Pancreatic function and diabetes](https://scholariq.org/topics/pancreatic-function-and-diabetes/)

## Paper topics

- [Pancreatic function and diabetes](https://scholariq.org/topics/pancreatic-function-and-diabetes/)
- [Glycogen Storage Diseases and Myoclonus](https://scholariq.org/topics/glycogen-storage-diseases-and-myoclonus/)
- [Metabolism and Genetic Disorders](https://scholariq.org/topics/metabolism-and-genetic-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.