For all of you who see Dr. Flanigan as well.
Latest Activity: Aug 19, 2017
This group does not have any discussions yet.
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?
Welcome toPPMD Community
Sign Upor Sign In
Or sign in with:
Need help using this community site? Visit Ning's Help Page.
April 21, 2018 all day – Charles F. Patton Middle School
© 2018 Created by PPMD.
Report an Issue |
Terms of Service
Please check your browser settings or contact your system administrator.