# Familial Hemiplegic Migraine and Episodic Ataxia Type-2 Are Caused by Mutations in the Ca2+ Channel Gene CACNL1A4

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/familial-hemiplegic-migraine-and-episodic-ataxia-type-2-are-caused-by-mutations/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Roel A. Ophoff,Gisela M. Terwindt,Monique N. Vergouwe,Ronald van Eijk,Peter J. Oefner,Susan M.G. Hoffman,Jane E. Lamerdin,Harvey W. Mohrenweiser,Dennis E. Bulman,Maurizio Ferrari,Joost Haan,Dick Lindhout,Gert‐Jan B. van Ommen,Marten H. Hofker,Michel D. Ferrari,Rune R. Frants |
| Citations | 2,343 |
| DOI | 10.1016/s0092-8674(00)81373-2 |
| Fields | Biochemistry, Genetics and Molecular Biology,Medicine,Neuroscience |
| Open Access | true |
| OA Status | bronze |
| OA URL | http://www.cell.com/article/S0092867400813732/pdf |
| OpenAlex ID | https://openalex.org/W2025197615 |
| PMID | 8898206 |
| Type | article |
| Year | 1996 |

## Paper authors

- [Maurizio Ferrari](https://scholariq.org/researchers/maurizio-ferrari/)

## Paper primary topic

- [Genetic Neurodegenerative Diseases](https://scholariq.org/topics/genetic-neurodegenerative-diseases/)

## Paper topics

- [Genetic Neurodegenerative Diseases](https://scholariq.org/topics/genetic-neurodegenerative-diseases/)
- [Mitochondrial Function and Pathology](https://scholariq.org/topics/mitochondrial-function-and-pathology/)
- [Neurological disorders and treatments](https://scholariq.org/topics/neurological-disorders-and-treatments/)

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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.