Boy with ultra-rare disease begins groundbreaking gene therapy

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  • เผยแพร่เมื่อ 14 ส.ค. 2022
  • After his parents desperately raised $3 million trying to find a cure for their son's rare genetic disease, Michael Pirovolakis is one step closer to possible recovery, beginning a groundbreaking clinical trial where he’s the only participant.
    #SPG50 #spasticparaplegia50 #genetherapy
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