L. Feng

Chemistry, structure and function of approved oligonucleotide therapeutics

Dilated cardiomyopathy: causes, mechanisms, and current and future treatment approaches

P.146Novel high-throughput digital analysis to quantify the amount of functional sarcolemmal dystrophin and myofibre regeneration in Duchenne muscular dystrophy clinical trial samples (exon 53 skipping with golodirsen)

Skeletal muscle pathology in autosomal dominant Emery‐Dreifuss muscular dystrophy with lamin A/C mutations