RettUK: 25 years closer to the cure
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“This work is combining improving diagnostic abilities with work that we hope will enable improved molecular research and understanding of what happens in the brain of people with Rett syndrome. This should also enable access to a good substitute for brain tissue”.

Professor Angus Clarke

  

Under the supervision of Professor Angus Clarke, Dr David Millar will continue research of the identification of mutations in the FOXG1 gene,


This project will work with the E-Rare project in Europe.