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A novel possible familial cause of epilepsy of infancy with migrating focal seizures related to SZT2 gene variant
Seizure threshold‐2 (SZT2) gene variants have been associated with a decrease in seizure threshold resulting in variable phenotypic expressions ranging from mild‐moderate intellectual disabilities without seizures, to an early‐onset epileptic encephalopathy with severe cognitive impairment. In addit...
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| Gepubliceerd in: | Epilepsia Open |
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| Hoofdauteurs: | , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
John Wiley and Sons Inc.
2021
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7918305/ https://ncbi.nlm.nih.gov/pubmed/33681650 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/epi4.12451 |
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