# Linkage of Benign Familial Infantile Convulsions to Chromosome 16p12-q12 Suggests Allelism to the Infantile Convulsions and Choreoathetosis Syndrome

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/linkage-of-benign-familial-infantile-convulsions-to-chromosome-16p12-q12/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Roberto Caraballo,Sylvana Pavek,Arnaud Lemainque,Marguerite Gastaldi,Bernard Échenne,Jacques Motté,Pierre Genton,Ricardo Cersósimo,Véronique Humbertclaude,Natalio Fejerman,Anthony P. Monaco,Mark G. Lathrop,Jacques Rochette,Pierre Szepetowski |
| Citations | 130 |
| DOI | 10.1086/318805 |
| Fields | Biochemistry, Genetics and Molecular Biology,Medicine |
| Open Access | true |
| OA Status | bronze |
| OA URL | http://www.cell.com/article/S000292970763119X/pdf |
| OpenAlex ID | https://openalex.org/W1971387228 |
| PMID | 11179027 |
| Type | article |
| Year | 2001 |

## Paper authors

- [Jacques Motté](https://scholariq.org/researchers/jacques-motte/)

## Paper primary topic

- [Epilepsy research and treatment](https://scholariq.org/topics/epilepsy-research-and-treatment/)

## Paper topics

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