Found: 6
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Function Over Form: Modeling Groups of Inherited Neurological Conditions in Zebrafish.
- Published in:
- Frontiers in Molecular Neuroscience, 2016, p. 1, doi. 10.3389/fnmol.2016.00055
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- Article
Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder.
- Published in:
- Nature Genetics, 2015, v. 47, n. 8, p. 926, doi. 10.1038/ng.3354
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- Article
The Expanding Role of MBD Genes in Autism: Identification of a MECP2 Duplication and Novel Alterations in MBD5, MBD6, and SETDB1.
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- Autism Research: Official Journal of the International Society for Autism Research, 2012, v. 5, n. 6, p. 385, doi. 10.1002/aur.1251
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- Article
Genetic compensation in a stable slc25a46 mutant zebrafish: A case for using F0 CRISPR mutagenesis to study phenotypes caused by inherited disease.
- Published in:
- PLoS ONE, 2020, v. 15, n. 3, p. 1, doi. 10.1371/journal.pone.0230566
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- Article
Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2.
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- Brain: A Journal of Neurology, 2014, v. 137, n. 1, p. 44, doi. 10.1093/brain/awt315
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- Article
Insights into the genotype‐phenotype correlation and molecular function of SLC25A46.
- Published in:
- Human Mutation, 2018, v. 39, n. 12, p. 1995, doi. 10.1002/humu.23639
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- Publication type:
- Article