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Idiopathic generalized epilepsy in a family with SCN4A‐related myotonia.
- Published in:
- Epilepsia Open, 2024, v. 9, n. 3, p. 951, doi. 10.1002/epi4.12920
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- Publication type:
- Article
A novel phenotype in an Italian family with a rare progranulin mutation.
- Published in:
- Journal of Neurology, 2022, v. 269, n. 11, p. 6170, doi. 10.1007/s00415-022-11285-7
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- Publication type:
- Article
Phenotypic Variability in Novel Doublecortin Gene Variants Associated with Subcortical Band Heterotopia.
- Published in:
- 2024
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- Publication type:
- Case Study