Landrum Peay, H., Fischer, R., Tzeng, J. P., Hesterlee, S. E., Morris, C., Strong Martin, A., . . . Mansfield, C. (2019). Gene therapy as a potential therapeutic option for Duchenne muscular dystrophy: A qualitative preference study of patients and parents. PLoS One.
Παραπομπή Chicago StyleLandrum Peay, Holly, et al. "Gene Therapy As a Potential Therapeutic Option for Duchenne Muscular Dystrophy: A Qualitative Preference Study of Patients and Parents." PLoS One 2019.
Παραπομπή MLALandrum Peay, Holly, et al. "Gene Therapy As a Potential Therapeutic Option for Duchenne Muscular Dystrophy: A Qualitative Preference Study of Patients and Parents." PLoS One 2019.
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