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Second Molecular Event Identification by Exome Sequencing for Intellectually Disabled Patients Carrying 16p13.11 CNVs — SEESIC  

Intellectual Disability Clinical Trial

Official title:
Second Molecular Event Identification by Exome Sequencing for Intellectually Disabled Patients Carrying 16p13.11 CNVs

Clinical Trial Summary

16p13.11 copy number variations are considered as predisposition factors for neurodevelopmental disorders but can be inherited from normal parents. SEESIC aims at identifying seond molecular events by exome sequencing that could modulate the phenotype and explain familial discrepancies.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03644797
Study type Observational
Source Hospices Civils de Lyon
Contact Nicolas CHATRON, MD
Phone 0472129697
Email nicolas.chatron@chu-lyon.fr
Status Not yet recruiting
Phase
Start date September 2018
Completion date March 2019
View Details
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