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CCG•CGG interruptions in high‐penetrance SCA8 families increase RAN translation and protein toxicity.
- Published in:
- EMBO Molecular Medicine, 2021, v. 13, n. 11, p. 1, doi. 10.15252/emmm.202114095
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- Article
Spectrin mutations cause spinocerebellar ataxia type 5.
- Published in:
- Nature Genetics, 2006, v. 38, n. 2, p. 184, doi. 10.1038/ng1728
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- Article
SCA8 CTG repeat: en masse contractions in sperm and intergenerational sequence changes may play a role in reduced penetrance.
- Published in:
- Human Molecular Genetics, 2000, v. 9, n. 14, p. 2125, doi. 10.1093/hmg/9.14.2125
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- Article
Reply?
- Published in:
- Nature Genetics, 2000, v. 24, n. 3, p. 215
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- Article
An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8).
- Published in:
- Nature Genetics, 1999, v. 21, n. 4, p. 379, doi. 10.1038/7710
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- Article
Comparison of expanded CAG repeat tracts in sperm and lymphocyte DNA from Machado Joseph disease and spinocerebellar ataxia type I patients.
- Published in:
- Human Mutation, 1998, v. 11, p. S74, doi. 10.1002/humu.1380110126
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- Article
CI-911: A placebo-controlled study in patients with primary degenerative dementia.
- Published in:
- Drug Development Research, 1988, v. 12, n. 3/4, p. 267, doi. 10.1002/ddr.430120309
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- Article