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HCFC1 variants in the proteolysis domain are associated with X‐linked idiopathic partial epilepsy: Exploring the underlying mechanism.
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- Clinical & Translational Medicine, 2023, v. 13, n. 6, p. 1, doi. 10.1002/ctm2.1289
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SZT2 variants associated with partial epilepsy or epileptic encephalopathy and the genotype-phenotype correlation.
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- Frontiers in Molecular Neuroscience, 2023, p. 01, doi. 10.3389/fnmol.2023.1162408
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- Article