Works matching IS 13646745 AND DT 2008 AND VI 9 AND IP 2
Results: 10
RNA interference of LRRK2–microarray expression analysis of a Parkinson’s disease key player.
- Published in:
- Neurogenetics, 2008, v. 9, n. 2, p. 83, doi. 10.1007/s10048-007-0114-0
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- Publication type:
- Article
Molecular evidence of founder effects of fatal familial insomnia through SNP haplotypes around the D178N mutation.
- Published in:
- Neurogenetics, 2008, v. 9, n. 2, p. 109, doi. 10.1007/s10048-008-0120-x
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- Publication type:
- Article
Is the early-onset torsion dystonia (EOTD) linked to TOR1A gene as frequent as expected in France?
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- Neurogenetics, 2008, v. 9, n. 2, p. 143, doi. 10.1007/s10048-008-0123-7
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- Publication type:
- Article
Long-range PCR for the diagnosis of spinocerebellar ataxia type 10.
- Published in:
- 2008
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- Publication type:
- Letter
Suggestive evidence for linkage for restless legs syndrome on chromosome 19p13.
- Published in:
- Neurogenetics, 2008, v. 9, n. 2, p. 75, doi. 10.1007/s10048-007-0113-1
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- Publication type:
- Article
Further examination of the candidate genes in chromosome 12p13 locus for late-onset Alzheimer disease.
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- Neurogenetics, 2008, v. 9, n. 2, p. 127, doi. 10.1007/s10048-008-0122-8
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- Publication type:
- Article
Novel NTRK1 mutations cause hereditary sensory and autonomic neuropathy type IV: demonstration of a founder mutation in the Turkish population.
- Published in:
- Neurogenetics, 2008, v. 9, n. 2, p. 119, doi. 10.1007/s10048-008-0121-9
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- Publication type:
- Article
Breakpoint characterization of a novel NF1 multiexonic deletion: a case showing expression of the mutated allele.
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- Neurogenetics, 2008, v. 9, n. 2, p. 95, doi. 10.1007/s10048-007-0115-z
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- Publication type:
- Article
Benign adult familial myoclonic epilepsy (BAFME): evidence of an extended founder haplotype on chromosome 2p11.1-q12.2 in five Italian families.
- Published in:
- Neurogenetics, 2008, v. 9, n. 2, p. 139, doi. 10.1007/s10048-008-0118-4
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- Publication type:
- Article
Structural genomic variation in ischemic stroke.
- Published in:
- Neurogenetics, 2008, v. 9, n. 2, p. 101, doi. 10.1007/s10048-008-0119-3
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- Publication type:
- Article