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...

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Bibliographische Detailangaben
Hauptverfasser: S. B. Artemyeva, О. А. Shidlovskaya, Yu. О. Papina, А. V. Monakhova, I. V. Shulyakov, D. V. Vlodavets
Format: Artikel
Sprache:Russisch
Veröffentlicht: ABV-press 2024-01-01
Schriftenreihe:Нервно-мышечные болезни
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Online-Zugang:https://nmb.abvpress.ru/jour/article/view/578
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