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Possibilities of molecular-genetic diagnosis of Duchenne/Becker myodystrophy
https://doi.org/10.25557/2073-7998.2020.04.73-74
Abstract
Clinical observation results of 13 patients with progressive Duchene/Becker muscular dystrophy are presented, molecular-genetic method is used in all cases.
About the Authors
N. V. Tkacheva
Astrakhan State Medical University of the Ministry of Healthcare of the Russian Federation
Russian Federation
Russian Federation
I. V. Soprunova
Astrakhan State Medical University of the Ministry of Healthcare of the Russian Federation
Russian Federation
Russian Federation
N. V. Androsova
Astrakhan State Medical University of the Ministry of Healthcare of the Russian Federation
Russian Federation
Russian Federation
I. A. Sinelnikova
Astrakhan State Medical University of the Ministry of Healthcare of the Russian Federation
Russian Federation
Russian Federation
V. V. Belopasov
Astrakhan State Medical University of the Ministry of Healthcare of the Russian Federation
Russian Federation
Russian Federation
A. V. Rakitskaya
Astrakhan State Medical University of the Ministry of Healthcare of the Russian Federation
Russian Federation
Russian Federation
Review
For citations:
Tkacheva N.V., Soprunova I.V., Androsova N.V., Sinelnikova I.A., Belopasov V.V., Rakitskaya A.V. Possibilities of molecular-genetic diagnosis of Duchenne/Becker myodystrophy. Medical Genetics. 2020;19(4):73-74. (In Russ.) https://doi.org/10.25557/2073-7998.2020.04.73-74
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