Works matching IS 13646745 AND DT 2004 AND VI 5 AND IP 2
Results: 8
Evidence for a modifier of onset age in Huntington disease linked to the HD gene in 4p16.
- Published in:
- Neurogenetics, 2004, v. 5, n. 2, p. 109, doi. 10.1007/s10048-004-0175-2
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- Article
Evidence of linkage and association on chromosome 20 for late-onset Alzheimer disease.
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- Neurogenetics, 2004, v. 5, n. 2, p. 121, doi. 10.1007/s10048-004-0174-3
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- Article
Towards a transcriptome definition of microglial cells.
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- Neurogenetics, 2004, v. 5, n. 2, p. 95, doi. 10.1007/s10048-004-0172-5
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- Article
Mitotic impairment by doublecortin is diminished by doublecortin mutations found in patients.
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- Neurogenetics, 2004, v. 5, n. 2, p. 83, doi. 10.1007/s10048-004-0176-1
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- Article
Mutations of the MTHFR gene (428C>T and [458G>T+459C>T]) markedly decrease MTHFR enzyme activity.
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- Neurogenetics, 2004, v. 5, n. 2, p. 135, doi. 10.1007/s10048-004-0177-0
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- Article
Sequence variation in the proximity of IDE may impact age at onset of both Parkinson disease and Alzheimer disease.
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- Neurogenetics, 2004, v. 5, n. 2, p. 115, doi. 10.1007/s10048-004-0173-4
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- Article
The estrogen receptor 1 G594A polymorphism is associated with migraine susceptibility in two independent case/control groups.
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- Neurogenetics, 2004, v. 5, n. 2, p. 129, doi. 10.1007/s10048-004-0181-4
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- Article
A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2.
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- Neurogenetics, 2004, v. 5, n. 2, p. 141, doi. 10.1007/s10048-004-0178-z
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- Article