Team
Alexandra Durr and Sandrine Humbert’s team focus on neurogenetic diseases, spinocerebellar degenerations (spastic paraplegias and cerebellar ataxias) and Huntington disease. These rare conditions share a late onset even though the mutant genes are expressed since conception and are critical for brain development. Our team showed that brain development is altered in Huntington disease, one of this rare inherited disease, and that these alterations contribute to the late onset.
Application
Sending a detailed CV including a list of publications, a brief outline of current research, scientific interests and career goals, as well as the name and contact details of references to alexandra.durr@icm-institute.org and sandrine.humbert@icm-institute.org
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