Found: 3
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Missense exchanges in the TTBK2 gene mutated in SCA11.
- Published in:
- Journal of Neurology, 2009, v. 256, n. 11, p. 1856, doi. 10.1007/s00415-009-5209-0
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- Publication type:
- Article
Early onset and slow progression of SCA28, a rare dominant ataxia in a large four-generation family with a novel AFG3L2 mutation.
- Published in:
- European Journal of Human Genetics, 2010, v. 18, n. 8, p. 965, doi. 10.1038/ejhg.2010.40
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- Publication type:
- Article
Two dominantly inherited ataxias linked to chromosome 16q22.1: SCA4 and SCA31 are not allelic.
- Published in:
- Journal of Neurology, 2011, v. 258, n. 7, p. 1223, doi. 10.1007/s00415-011-5905-4
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- Publication type:
- Article