Found: 3
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A novel composition of two heterozygous GFM1 mutations in a Chinese child with epilepsy and mental retardation.
- Published in:
- Brain & Behavior, 2020, v. 10, n. 10, p. 1, doi. 10.1002/brb3.1791
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- Publication type:
- Article
Novel and de novo point and large microdeletion mutation in PRRT2‐related epilepsy.
- Published in:
- Brain & Behavior, 2020, v. 10, n. 5, p. 1, doi. 10.1002/brb3.1597
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- Publication type:
- Article
A novel heterozygous ATP1A2 pathogenic variant in a Chinese child with MELAS‐like alternating hemiplegia.
- Published in:
- Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 5, p. 1, doi. 10.1002/mgg3.2146
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- Publication type:
- Article