Action Duchenne (formerly PPUK)

In Research

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The Action Duchenne website aims to offer a unique forum for sharing information and ideas in the search for a cure and better medical care for Duchenne and Becker and will at all times attempt to ensure postings are accurate, scientifically peer reviewed and not offensive to individuals. Action Duchenne, however, cannot take responsibility for personal opinions, information and the content of links to other websites. It is essential that you always contact your clinician or GP before taking any course of medication, therapy or supplement.

Aurelie Goyenvalle

Aurelie was the European Society for Gene Therapy young investigator of the year in 2005 when working in the DMD lab at Genethon Paris. Action Duchenne, Association Monegasque contre less Myopathies (AMM) and Parent Project France are now funding Aurelie to undertake an AAV/U7 research project with Professor Dame Kay Davies in her lab at Oxford University.

Recent comments

genmedlabmom wrote:

Hello! thank you for your post! But I have a question. Does not the AAV viral......

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Mark Silverman wrote:

Aurelie This looks very interesting, particularly given that you are looking for a......

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