Found: 4
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Functional Investigation of TUBB4A Variants Associated with Different Clinical Phenotypes.
- Published in:
- Molecular Neurobiology, 2022, v. 59, n. 8, p. 5056, doi. 10.1007/s12035-022-02900-9
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- Publication type:
- Article
West Syndrome Caused By a Chloride/Proton Exchange-Uncoupling CLCN6 Mutation Related to Autophagic-Lysosomal Dysfunction.
- Published in:
- Molecular Neurobiology, 2021, v. 58, n. 6, p. 2990, doi. 10.1007/s12035-021-02291-3
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- Publication type:
- Article
The Glycosylphosphatidylinositol biosynthesis pathway in human diseases.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Large heterozygous deletion and uniparental disomy masquerading as homozygosity in CHKB gene.
- Published in:
- Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 7, p. 1, doi. 10.1002/mgg3.2162
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- Publication type:
- Article