# PRRT2 Mutations are the major cause of benign familial infantile seizures

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/prrt2-mutations-are-the-major-cause-of-benign-familial-infantile-seizures/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Julian Schubert,Roberta Paravidino,Felicitas Becker,Andrea Berger,Nerses Bebek,Amedeo Bianchi,Knut Brockmann,Giuseppe Capovilla,Bernardo Dalla Bernardina,Yukio Fukuyama,Georg F. Hoffmann,Karin Jurkat‐Rott,Anna-Kaisa Anttonen,Gerhard Kurlemann,Anna-Elina Lehesjoki,Frank Lehmann‐Horn,Massimo Mastrangelo,Ulrike Mause,Stephan A. Müller,Bernd A. Neubauer,B Püst,D. Rating,Angela Robbiano,Susanne Ruf,Christopher Schroeder,Andreas Seidel,Nicola Specchio,Ulrich Stephani,Pasquale Striano,Jens Teichler,Dilşad Türkdoğan,Federico Vigevano,Maurizio Viri,Peter Bauer,Federico Zara,Holger Lerche,Yvonne Weber |
| Citations | 107 |
| DOI | 10.1002/humu.22126 |
| Fields | Biochemistry, Genetics and Molecular Biology,Medicine |
| Open Access | false |
| OA Status | closed |
| OpenAlex ID | https://openalex.org/W2009308037 |
| PMID | 22623405 |
| Type | article |
| Year | 2012 |

## Paper authors

- [Nerses Bebek](https://scholariq.org/researchers/nerses-bebek/)

## 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 Transport and Channel Regulation](https://scholariq.org/topics/ion-transport-and-channel-regulation/)

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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.