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Muscular dystrophy associated with the DMD gene in women
Vorontsova E.O., Zinina A.V., Shchagina O.A.
Possibility of exon skipping therapy for Duchenne muscular dystrophy in Russian patients: present and future
Zinina E.V., Bulakh M.V., Ryzhkova O.P., Shchagina O.A., Polyakov A.V.
Stages of research and development of therapeutic approaches for Duchenne myodystrophy. Part II: etiotropic approaches
Kochergin-Nikitskiy K.S., Smirnikhina S.A., Lavrov A.V.
Stages of research and development of therapeutic approaches for Duchenne myodystrophy. Part I: the period before etiotropic approaches introduction
Kochergin-Nikitskiy K.S., Smirnikhina S.A., Lavrov A.V.
Modern methods of therapy of Duchenne muscular dystrophy: literature review with a clinical case
Artemyeva S.B., Shidlovskaya О.А., Papina Y.О., Monakhova А.V., Shulyakov I.V., Vlodavets D.V.
Change in the spectrum of detected mutations in the DMD gene depending on the methodological capabilities of the laboratory
Zinina E.V., Bulakh M.V., Ryzhkova O.P., Shchagina O.A., Polyakov A.V.
Comparative analysis of phenotypes features in two common genetic variants of limb-girdle muscular dystrophy
Sharkova I.V., Dadali E.L., Ugarov I.V., Ryzhkova O.P., Polyakov A.V.
Positive experience in treating patients with Duchenne muscular dystrophy caused by a nonsense mutation: family clinical case
Kraeva L.S., Fadeeva E.V.
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