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| Genetic Epilepsy v2.9 | SOX10 | Lucy Spencer Classified gene: SOX10 as Green List (high evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genetic Epilepsy v2.9 | SOX10 | Lucy Spencer Gene: sox10 has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genetic Epilepsy v2.8 | SOX10 |
Lucy Spencer gene: SOX10 was added gene: SOX10 was added to Genetic Epilepsy. Sources: Literature Mode of inheritance for gene: SOX10 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: SOX10 were set to 29792164; 35725288 Phenotypes for gene: SOX10 were set to PCWH syndrome MIM#609136 Review for gene: SOX10 was set to GREEN Added comment: Seizures are a rare feature of this disorder and may be caused by the delayed myelination/demyelination associated with this gene. There are several reports in the literature of individuals with seizures as part of PCWH syndrome (PMIDs: 29792164, 35725288). Sources: Literature |
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