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Dr Steven Gray talks about AAV gene therapy that can potentially help AHC patients.

Posted on November 4, 2018 By siggi


Dr. Steven Gray is one of the world leaders in developing gene therapies for rare and ultra-rare diseases. He works at the University of Texas Southwestern, where he is currently an Associate Professor in the Department of Pediatrics at the University of Texas Southwestern Medical Center.

Interviews Tags:aav, agusta fanney, AHC, ahcim, gene therapy, siggi johannesson, steven gray

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