- Role of Olig1 and Olig2 in Down syndrome.
- TUBA1A mutations cause wide spectrum lissencephaly.
- Cell cloning-based transcriptome analysis in Rett patients.
Neonatal epilepsies with suppression burst pattern are rare, especially the forms with normal MRI and normal metabolic screening. This is the reason why we are looking for additional cases to increase the size of our cohort and to go faster in the identification of genetic causes for these diseases. As of september 2009, we have collected biological samples for 27 cases.
We invite all interested colleagues to join this project and collaborate.
To participate, we invite you to contact us via the contact form or via e-mail sent to Dr Mathieu Milh, coordinator of the study. We will be pleased to provide you with any additional information you may need.
Please contact us before sending any biological material since we are following very strict rules to comply with the french regulations.