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Gene therapy as a potential therapeutic option for Duchenne muscular dystrophy: A qualitative preference study of patients and parents

OBJECTIVES: Duchenne muscular dystrophy (DMD) is a rare neuromuscular disorder that causes progressive weakness and early death. Gene therapy is an area of new therapeutic development. This qualitative study explored factors influencing parents’ and adult patients’ preferences about gene therapy. ME...

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Τόπος έκδοσης:	PLoS One
Κύριοι συγγραφείς:	Landrum Peay, Holly, Fischer, Ryan, Tzeng, Janice P., Hesterlee, Sharon E., Morris, Carl, Strong Martin, Amy, Rensch, Colin, Smith, Edward, Ricotti, Valeria, Beaverson, Katherine, Wand, Hannah, Mansfield, Carol
Μορφή:	Artigo
Γλώσσα:	Inglês
Έκδοση:	Public Library of Science 2019
Θέματα:	Research Article
Διαθέσιμο Online:	https://ncbi.nlm.nih.gov/pmc/articles/PMC6493713/ https://ncbi.nlm.nih.gov/pubmed/31042754 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0213649
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Gene therapy as a potential therapeutic option for Duchenne muscular dystrophy: A qualitative preference study of patients and parents

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