Modern methods of therapy of Duchenne muscular dystrophy: literature review with a clinical case
Duchenne muscular dystrophy is a genetic, X-linked, relentlessly progressive disease. Due to a genetic defect, the reading frame is disrupted during the synthesis of the dystrophin protein, resulting in its loss of functionality. As a result of the absence of dystrophin, there is a gradual destructi...
| Päätekijät: | , , , , , |
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| Aineistotyyppi: | Artikkeli |
| Kieli: | Russian |
| Julkaistu: |
ABV-press
2024-01-01
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| Sarja: | Нервно-мышечные болезни |
| Aiheet: | |
| Linkit: | https://nmb.abvpress.ru/jour/article/view/578 |