Genetic Analysis of Children with Dravet Syndrome in a Resourcelimited Setting
Objective: To identify the common causal gene mutations in Thai children with the Dravet (DS) phenotype, using single gene analysis. Material and Methods: The study was carried out on 20 DS patients at Siriraj Hospital, Bangkok, Thailand. Sanger sequencing of the Voltage-Gated Sodium Channel Alpha S...
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| Main Authors: | , , , |
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| Other Authors: | |
| Format: | Article |
| Published: |
2022
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| Subjects: | |
| Online Access: | https://repository.li.mahidol.ac.th/handle/123456789/74580 |
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| Institution: | Mahidol University |