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Autor:
Aleksey A. Pushkov, Alexey Kurenkov, Tatyana Podkletnova, Olga B. Kondakova, Lale A. Pak, Iulia I. Davydova, Dmitry I. Grebenkin, Kirill Savostyanov, L. M. Kuzenkova, Anastasiya A. Lyalina, Bella Bursagova
Publikováno v:
L.O. Badalyan Neurological Journal. 2:159-166
Duchenne muscular dystrophy (DMD) is a disease with an X-linked recessive type of inheritance, belonging to a group of disorders with primary muscle damage, caused by pathogenic variants in the DMD gene and associated with dysfunction of the dystroph