For all of you who see Dr. Flanigan as well.
Latest Activity: Feb 11
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We are based in NZ,my son has duplication for exon 41
We have never seen Dr Flaingan,however we are waiting anxiously for his research to proceed and get a green light
I saw last webinar about duplication research and it was very promising
Hi, we don't see Dr. Flanigan in person, but my daughter is in the United Dystrophinopathy Project. Nationwide Childrens Hospital & Dr Flanigan are the ones who did her DNA analysis which showed duplication of exxon 8-17. Is anyone else involved in that study?
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