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Lack of Implication for CALHM1 P86L Common Variation in Italian Patients with Early and Late Onset Alzheimer’s Disease
- Publication Year :
- 2010
-
Abstract
- A recent study identified a polymorphism (Pro86Leu) in the Calcium homeostasis modulator 1 (CALHM1) gene whose minor Leucine allele showed a higher frequency in Alzheimer's disease (AD) patients compared to controls (29% in AD and 22% in controls). Further studies provided conflicting results in different ethnic groups. In order to assess the involvement of the CALHM1 genetic variant on the risk of developing AD, we analyzed the genotype and allele distributions of the Pro86Leu polymorphism in 758 Italian subjects. Our results did not confirm an association between the CALHM1 variation and AD, thus suggesting a genetic heterogeneity among the various populations.
- Subjects :
- Male
Genotype
Proline
DNA Mutational Analysis
Late onset
Disease
Biology
Polymorphism, Single Nucleotide
Gene Frequency
Polymorphism (computer science)
Alzheimer Disease
Leucine
Humans
Allele
Age of Onset
Gene
Aged
apolipoprotein E
Membrane Glycoproteins
Genetic heterogeneity
General Neuroscience
General Medicine
calcium homeostasis modulator 1
Middle Aged
Alzheimer's disease
Alzheimer's disease, apolipoprotein E, calcium homeostasis modulator 1, genetic variation
Psychiatry and Mental health
Clinical Psychology
Italy
Immunology
genetic variation
CALHM1
Female
Calcium Channels
Geriatrics and Gerontology
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Accession number :
- edsair.doi.dedup.....0531dad278188c994dc061782e427c78