Identification of the molecular basis of premature atherosclerosis in high penetrance pedigrees
- Conditions
- atherosclerosiscardiovascular disease1000751010003216
- Registration Number
- NL-OMON33048
- Lead Sponsor
- Academisch Medisch Centrum
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 1000
Inclusion Criteria
Member of high penetrence family for cardiovascular disease
Exclusion Criteria
None
Study & Design
- Study Type
- Observational invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>A) Identification of sequence variations resulting in CVD in pedigrees<br /><br>B) Determining through which mechanism sequence variations result in disease.</p><br>
- Secondary Outcome Measures
Name Time Method <p>none</p><br>