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Clinical Trial Summary

This study will focus on a large cohort of multiplex families, to precisely identify candidate genes. The fact of have a large database (fifty families, collected by the principal investigator for more than two decades), will contribute to the discovery of genes of interest. It will also allow testing for the presence or absence of mutations found in other cohorts in previous studies. The main objective of this study is to identify genetic abnormalities associated with the presence and severity of idiopathic scoliosis, in families of scoliosis.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05116436
Study type Observational
Source Ramsay Générale de Santé
Contact Jean-François Oudet
Phone 0683346567
Email jf.oudet@ecten.eu
Status Recruiting
Phase
Start date June 6, 2020
Completion date June 6, 2022

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