Duchenne Muscular Dystrophy: Ryan's Story

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  • เผยแพร่เมื่อ 17 ก.ย. 2024
  • Learn more about Duchenne Muscular Dystrophy (bit.ly/1yzusRh) or connect with a specialist: (bit.ly/1xz0Cy1).
    Donate now: bit.ly/1NDRyBQ
    Learn about our Muscular Dystrophy Research (here: bit.ly/1yzuys7) and our Center for Gene Therapy (here: bit.ly/1yzuCbf). Meet Dr. Mendell (here: bit.ly/1yzuPLv).
    Duchenne muscular dystrophy (DMD) is the most common life-threatening childhood form of muscular dystrophy. As it is caused by genetic defects that lead to missing or non-functional proteins, faculty members are investigating the possibility of gene replacement or gene therapy as treatment options for DMD.

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