Found: 7
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Heterozygous PGM3 Variants Are Associated With Idiopathic Focal Epilepsy With Incomplete Penetrance.
- Published in:
- Frontiers in Genetics, 2020, v. 11, p. N.PAG, doi. 10.3389/fgene.2020.559080
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- Publication type:
- Article
UNC13B variants associated with partial epilepsy with favourable outcome.
- Published in:
- 2021
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- Publication type:
- journal article
CELSR1 variants are associated with partial epilepsy of childhood.
- Published in:
- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2022, v. 189, n. 7/8, p. 247, doi. 10.1002/ajmg.b.32916
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- Publication type:
- Article
Few individuals with Lennox-Gastaut syndrome have autism spectrum disorder: a comparison with Dravet syndrome.
- Published in:
- Journal of Neurodevelopmental Disorders, 2018, v. 10, n. 1, p. 1, doi. 10.1186/s11689-018-9229-x
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- Publication type:
- Article
SHROOM4 Variants Are Associated With X-Linked Epilepsy With Features of Generalized Seizures or Generalized Discharges.
- Published in:
- Frontiers in Molecular Neuroscience, 2022, v. 15, p. 1, doi. 10.3389/fnmol.2022.862480
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- Publication type:
- Article
CACNA1A Mutations Associated With Epilepsies and Their Molecular Sub-Regional Implications.
- Published in:
- Frontiers in Molecular Neuroscience, 2022, v. 15, p. 1, doi. 10.3389/fnmol.2022.860662
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- Publication type:
- Article
A Point Mutation in SCN1A 5′ Genomic Region Decreases the Promoter Activity and Is Associated with Mild Epilepsy and Seizure Aggravation Induced by Antiepileptic Drug.
- Published in:
- Molecular Neurobiology, 2017, v. 54, n. 4, p. 2428, doi. 10.1007/s12035-016-9800-y
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- Publication type:
- Article