# The clinical utility of an <i>SCN1A</i> genetic diagnosis in infantile‐onset epilepsy

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/the-clinical-utility-of-an-i-scn1a-i-genetic-diagnosis-in-infantile-onset/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Andreas Brunklaus,Liam Dorris,Rachael Ellis,Eleanor Reavey,Elizabeth Lee,GORDON FORBES,Richard Appleton,J. Helen Cross,Colin D. Ferrie,Imelda Hughes,Alice Jollands,Mary D. King,John Livingston,Bryan Lynch,Sunny Philip,Ingrid E. Scheffer,Ruth Williams,Sameer M. Zuberi |
| Citations | 69 |
| DOI | 10.1111/dmcn.12030 |
| Fields | Biochemistry, Genetics and Molecular Biology,Medicine |
| Open Access | true |
| OA Status | bronze |
| OA URL | https://onlinelibrary.wiley.com/doi/pdfdirect/10.1111/dmcn.12030 |
| OpenAlex ID | https://openalex.org/W1983334701 |
| PMID | 23163885 |
| Type | article |
| Year | 2012 |

## Paper authors

- [Liam Dorris](https://scholariq.org/researchers/liam-dorris/)

## Paper journal

- [Developmental Medicine & Child Neurology](https://scholariq.org/journals/developmental-medicine-and-child-neurology/)

## 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/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Ion channel regulation and function](https://scholariq.org/topics/ion-channel-regulation-and-function/)

---
Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.