Found: 7
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Variants in BRWD3 associated with X‐linked partial epilepsy without intellectual disability.
- Published in:
- CNS Neuroscience & Therapeutics, 2023, v. 29, n. 2, p. 727, doi. 10.1111/cns.14057
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- 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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- Article
Recessive PKD1 Mutations Are Associated With Febrile Seizures and Epilepsy With Antecedent Febrile Seizures and the Genotype-Phenotype Correlation.
- Published in:
- Frontiers in Molecular Neuroscience, 2022, v. 15, p. 1, doi. 10.3389/fnmol.2022.861159
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- Article
Recessive LAMA5 Variants Associated With Partial Epilepsy and Spasms in Infancy.
- Published in:
- Frontiers in Molecular Neuroscience, 2022, v. 15, p. 1, doi. 10.3389/fnmol.2022.825390
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- 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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- 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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- Article
Optimization of in silico tools for predicting genetic variants: individualizing for genes with molecular sub-regional stratification.
- Published in:
- Briefings in Bioinformatics, 2020, v. 21, n. 5, p. 1776, doi. 10.1093/bib/bbz115
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- Article