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Biological effects of the PINK1 c.1366C>T mutation: implications in Parkinson disease pathogenesis.
- Published in:
- Neurogenetics, 2007, v. 8, n. 2, p. 103, doi. 10.1007/s10048-006-0072-y
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- Article
A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson’s disease risk in Taiwan.
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- Neurogenetics, 2006, v. 7, n. 3, p. 133, doi. 10.1007/s10048-006-0041-5
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- Article
Early-onset Parkinson's disease caused by a novel parkin mutation in a genetic isolate from north-eastern Brazil.
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- Neurogenetics, 2006, v. 7, n. 1, p. 13, doi. 10.1007/s10048-005-0017-x
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- Article
Comprehensive analysis of the LRRK2 gene in sixty families with Parkinson's disease.
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- European Journal of Human Genetics, 2006, v. 14, n. 3, p. 322, doi. 10.1038/sj.ejhg.5201539
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- Article
Homozygous PINK1 C‐terminus mutation causing early‐onset parkinsonism.
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- Annals of Neurology, 2004, v. 56, n. 3, p. 427
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- Article