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Clinical Trial Summary

The mechanism of the majority of the dyslipidemia is multifactorial at the molecular level and remains elusive in more than 50% of the patients in many clinical conditions. Next generation sequencing, a booming strategy, improves the molecular diagnosis efficiency in both monogenic and polygenic dyslipidemia.

In order to decipher the mechanisms involved in the occurrence of dyslipidemia, in addition to the exploration of known candidate genes and Single Nucleotide Polymorphisms (SNP) involved in polygenic modulation, new genes involved in the regulation of lipoprotein metabolism or associated with lipids concentrations need to be sequenced in large groups of dyslipidemic patients.

The goal of this project is to gain new insight into genotype/phenotype correlation.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03939039
Study type Observational
Source Hospices Civils de Lyon
Contact Mathilde Di Filippo
Phone 4 72 11 89 94
Email mathilde.di-filippo@chu-lyon.fr
Status Recruiting
Phase
Start date January 1, 2000
Completion date January 1, 2025

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