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Homozygous TBC1D24 Mutation in a Case of Epilepsia Partialis Continua
TBC1D24 mutation-related epileptic syndrome includes a wide spectrum of epilepsies. We describe a case with a homozygous TBC1D24 mutation inherited from consanguineous parents. The patient manifested epilepsia partialis continua (EPC) and rare secondary generalized tonic–clonic seizure without intel...
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| izdano v: | Front Neurol |
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| Main Authors: | , , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Frontiers Media S.A.
2018
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5787533/ https://ncbi.nlm.nih.gov/pubmed/29416524 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fneur.2017.00750 |
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