This Blog was created for people interested in Friedreich Ataxia in South Australia. It provides a relaxing place to share and communicate what is going on, as well as links to FA groups and information from around the world. FAinSA is a non medical site for patients, families and friends of FA. All comments are a purely personal nature and do not replace advice from trained medical professionals
Friday, March 12, 2010
I saw this on Times Online and thought you might be interested
Gene therapy for spinal muscular atrophy could be tested in 2 years
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