Disease: Limb-girdle muscular dystrophy- type 2C
- A gene-edited mouse model of limb-girdle muscular dystrophy 2C for testing exon skipping
- Aberrant Adenosine Triphosphate Release and Impairment of P2Y2-Mediated Signaling in Sarcoglycanopathies
- Childhood onset limb-girdle muscular dystrophies in the Aegean part of Turkey
- Circulating Biomarkers in Muscular Dystrophies: Disease and Therapy Monitoring
- Clinical and genetic spectrum of sarcoglycanopathies in a large cohort of Chinese patients
- Current Genetic Survey and Potential Gene-Targeting Therapeutics for Neuromuscular Diseases
- Designing Effective Antisense Oligonucleotides for Exon Skipping
- Dilated cardiomyopathy and limb-girdle muscular dystrophy-dystroglycanopathy due to novel pathogenic variants in the DPM3 gene
- Efficient exon skipping of SGCG mutations mediated by phosphorodiamidate morpholino oligomers
- Immunohistochemistry of sarcolemmal membrane-associated proteins in formalin-fixed and paraffin-embedded skeletal muscle tissue: a promising tool for the diagnostic evaluation of common muscular dystrophies
- Intrafamilial variability of limb-girdle muscular dystrophy, LGMD1D type
- Involvement of muscle satellite cell dysfunction in neuromuscular disorders: Expanding the portfolio of satellite cell-opathies
- LGMD. Identification, description and classification
- Natural History of Cardiac and Respiratory Involvement, Prognosis and Predictive Factors for Long-Term Survival in Adult Patients with Limb Girdle Muscular Dystrophies Type 2C and 2D
- Recent advancements in exon-skipping therapies using antisense oligonucleotides and genome editing for the treatment of various muscular dystrophies
- Sarcoglycanopathies: an update
- Severe murine limb-girdle muscular dystrophy type 2C pathology is diminished by FTY720 treatment
- Systemic γ-sarcoglycan AAV gene transfer results in dose-dependent correction of muscle deficits in the LGMD 2C/R5 mouse model
- Targeted next-generation sequencing determined a novel <em>SGCG</em> variant that is associated with limb-girdle muscular dystrophy type 2C: A case report
- Targeted next-generation sequencing determined a novel SGCG variant that is associated with limb-girdle muscular dystrophy type 2C: A case report
- Three siblings with variable degrees of neuromuscular involvement and congenital sideroblastic anemia: A peculiar phenotype and a surprise genotypic explanation
- Tips to Design Effective Splice-Switching Antisense Oligonucleotides for Exon Skipping and Exon Inclusion
- γ-sarcoglycan and dystrophin mutation spectrum in an Algerian cohort