Identification of hub genes and therapeutic siRNAs to develop novel adjunctive therapy for Duchenne muscular dystrophy

Abstract Objective Duchenne muscular dystrophy (DMD) is a devastating X-linked neuromuscular disorder caused by various defects in the dystrophin gene and still no universal therapy. This study aims to identify the hub genes unrelated to excessive immune response but responsible for DMD progression...

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Bibliographic Details
Published in:BMC Musculoskeletal Disorders
Main Authors: Na Li, Zhikai Xiahou, Zhuo Li, Zilian Zhang, Yafeng Song, Yongchun Wang
Format: Article
Language:English
Published: BMC 2024-05-01
Subjects:
Online Access:https://doi.org/10.1186/s12891-024-07206-6