Associated Papers
Combinatorial activation of the WNT-dependent fibrogenic program by distinct complement subunits in dystrophic muscle.
Florio F et al.
Embo Molecular Medicine, 2023
37927228 (PubMed )
Supplement: EMMM-15-e17405-s002.pdf
Comprehensive genetic analysis of 961 unrelated Duchenne Muscular Dystrophy patients: Focus on diagnosis, prevention and therapeutic possibilities.
Kumar SH et al.
Plos One, 2020
Clinical and molecular characterization of a cohort of patients with novel nucleotide alterations of the Dystrophin gene detected by direct sequencing.
Magri F et al.
Bmc Medical Genetics, 2011
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