A Review of Genetic Etiology and Emerging Molecular Therapies for FSHD in Preclinical Studies

Mohammad Reza Seyyed Taghia; Reza Jafarzadeh Esfehani; Reza Boostani; Mohammad Shariati; Ariane Sadr Nabavi

Volume 8, Issue 1 , March 2021, , Pages 35-40


  Facioscapulohumeral muscular dystrophy is one of the most common musculoskeletal diseases with a considerable burden. Most of the affected individuals experience muscle weakness as the common muscular symptom. Despite the underlying genetic mechanism which is extensively studied, curative treatment is ...  Read More