# The tumour suppressor gene WWOX is mutated in autosomal recessive cerebellar ataxia with epilepsy and mental retardation

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/the-tumour-suppressor-gene-wwox-is-mutated-in-autosomal-recessive-cerebellar/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Martial Mallaret,Matthis Synofzik,Jae‐Ho Lee,Cari A. Sagum,Muhammad Mahajnah,Rajech Sharkia,Nathalie Drouot,M. Renaud,Fabrice Klein,Mathieu Anheim,Christine Tranchant,Cyril Mignot,Jean‐Louis Mandel,Mark T. Bedford,Peter Bauer,Mustafa A. Salih,Rebecca Schüle,Lüdger Schöls,C. Marcelo Aldaz,Michel Kœnig |
| Citations | 132 |
| DOI | 10.1093/brain/awt338 |
| Fields | Biochemistry, Genetics and Molecular Biology,Medicine,Neuroscience |
| Open Access | true |
| OA Status | bronze |
| OA URL | https://academic.oup.com/brain/article-pdf/137/2/411/13797939/awt338.pdf |
| OpenAlex ID | https://openalex.org/W2171830224 |
| PMID | 24369382 |
| Type | article |
| Year | 2013 |

## Paper authors

- [Jae‐Ho Lee](https://scholariq.org/researchers/jae-ho-lee/)

## Paper journal

- [Brain](https://scholariq.org/journals/brain/)

## Paper primary topic

- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)

## Paper topics

- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)
- [Nuclear Receptors and Signaling](https://scholariq.org/topics/nuclear-receptors-and-signaling/)
- [Moyamoya disease diagnosis and treatment](https://scholariq.org/topics/moyamoya-disease-diagnosis-and-treatment/)

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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.