The Genetic & Development of Cardiac Defect team publishes a new study in eLife
The Genetic & Development of Cardiac Defect team publishes a new study in eLife
The Human Neurogenetics team contributes to the description of 17 new patients.
The study of a micro-rearragement in a patient with polymicrogyria allows the Human Neurogenetics team to show that the...
It is the first knock-in model based on a recurrent pathogenic variant in Kcnq2.
The MMG is recruiting a Bioinformatics Engineer in high throughput sequencing data analysis for its Genomics and...
Our laboratory has just reported a very unusual and never described phenotype associated with a mutation of the GLE1...
The study is published in EMBO Molecular Medicine.
The Bioinformatics & Genetics team together with the NeuroMyology Translational team published a tool for rapidly...
The Human Neurogenetics team has discovered a new genetic cause for Aicardi syndrome, also called early myoclonic...
Desipramine was shown to reduce apneas in a model of RTT. A phase 2 trial was performed in 36 girls with RTT.