Plateforme Mutations

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High throughput sequencing and Rare Diseases "Plateforme Mutations" initiative. Understanding the molecular basis of human diseases of genetic origin is far from being achieved. It remains, in particular, to identify the genes that are the most rarely involved. Identification of these genes is of paramount importance to elucidate the pathogenic mechanisms of the diseases and for the development of diagnostic tools and of innovative therapeutics.

Contact information:

http://www.cns.fr/spip/High-throughput-sequencing-and.html

The fund is not a competitive fund
web site: http://www.cns.fr/spip/High-throughput-sequencing-and.html