Works matching IS 13646745 AND DT 2005 AND VI 6 AND IP 2
Results: 9
A novel NIPA1 mutation associated with a pure form of autosomal dominant hereditary spastic paraplegia.
- Published in:
- Neurogenetics, 2005, v. 6, n. 2, p. 79, doi. 10.1007/s10048-004-0209-9
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- Publication type:
- Article
Novel G335V mutation in the tau gene associated with early onset familial frontotemporal dementia.
- Published in:
- 2005
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- Publication type:
- Letter
Creutzfeldt-Jakob disease associated with an R148H mutation of the prion protein gene.
- Published in:
- 2005
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- Publication type:
- Letter
Screening of the regulatory and coding regions of vascular endothelial growth factor in amyotrophic lateral sclerosis.
- Published in:
- 2005
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- Publication type:
- Letter
Novel mutations and repeated findings of mutations in familial Alzheimer disease.
- Published in:
- Neurogenetics, 2005, v. 6, n. 2, p. 85, doi. 10.1007/s10048-005-0211-x
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- Publication type:
- Article
The urokinase-plasminogen activator (PLAU) gene is not associated with late onset Alzheimer’s disease.
- Published in:
- 2005
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- Publication type:
- Correction Notice
LGI1: a gene involved in epileptogenesis and glioma progression?
- Published in:
- Neurogenetics, 2005, v. 6, n. 2, p. 59, doi. 10.1007/s10048-005-0216-5
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- Publication type:
- Article
Diagnosis of Pelizaeus–Merzbacher disease: detection of proteolipid protein gene copy number by real-time PCR.
- Published in:
- Neurogenetics, 2005, v. 6, n. 2, p. 73, doi. 10.1007/s10048-005-0214-7
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- Publication type:
- Article
A genome-wide scan provides evidence for loci influencing a severe heritable form of common migraine.
- Published in:
- Neurogenetics, 2005, v. 6, n. 2, p. 67, doi. 10.1007/s10048-005-0215-6
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- Publication type:
- Article