# A Wide Spectrum of Genetic Disorders Causing Severe Childhood Epilepsy in Taiwan: A Case Series of Ultrarare Genetic Cause and Novel Mutation Analysis in a Pilot Study

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/a-wide-spectrum-of-genetic-disorders-causing-severe-childhood-epilepsy-in-taiwan/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Syuan‐Yu Hong,Jiann‐Jou Yang,Shuan‐Yow Li,Inn‐Chi Lee |
| Citations | 27 |
| DOI | 10.3390/jpm10040281 |
| Fields | Biochemistry, Genetics and Molecular Biology,Medicine |
| Open Access | true |
| OA Status | gold |
| OA URL | https://www.mdpi.com/2075-4426/10/4/281/pdf?version=1608021032 |
| OpenAlex ID | https://openalex.org/W3110935433 |
| PMID | 33333793 |
| Type | article |
| Year | 2020 |

## Paper authors

- [Syuan‐Yu Hong](https://scholariq.org/researchers/syuan-yu-hong/)

## Paper journal

- [Journal of Personalized Medicine](https://scholariq.org/journals/journal-of-personalized-medicine/)

## Paper primary topic

- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)

## Paper topics

- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Epilepsy research and treatment](https://scholariq.org/topics/epilepsy-research-and-treatment/)
- [Glycogen Storage Diseases and Myoclonus](https://scholariq.org/topics/glycogen-storage-diseases-and-myoclonus/)

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