Skip to content
2000
Volume 7, Issue 3
  • ISSN: 1389-2002
  • E-ISSN: 1875-5453

Abstract

Alzheimer's disease (AD) is a genetically complex and heterogenous disorder. In a small proportion of cases, mutations in three determinative (causal) genes are responsible for autosomal dominant early-onset forms of AD. The majority of cases, however, is sporadic, late-onset AD with unknown etiology. The pathology and clinical manifestations of these forms are influenced by multiple genetic and environmental risk factors. Over the past decades, a number of candidate genes have been identified as disease modifiers with conflicting results. This study reviews susceptibility genes that are associated with increased risk of developing AD.

Loading

Article metrics loading...

/content/journals/cdm/10.2174/138920006776359257
2006-04-01
2025-09-14
Loading full text...

Full text loading...

/content/journals/cdm/10.2174/138920006776359257
Loading
This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error
Please enter a valid_number test