Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
Human Mutation|June 20, 2020
A single c.1715G>C calpain 3 gene variant causes dominant calpainopathy with loss of calpain 3 expression and activityJohn Vissing, Julia R Dahlqvist, Carinne Roudaut, et al.
Neuromuscular Disorders : NMD|March 20, 2021
Late-onset camptocormia caused by a heterozygous in-frame CAPN3 deletionMarco Spinazzi, Jerome Poupiot, Julien Cassereau, et al.
Life Science Alliance|October 20, 2022
Dlk1-Dio3 cluster miRNAs regulate mitochondrial functions in the dystrophic muscle in Duchenne muscular dystrophyAi Vu Hong, Nathalie Bourg, Peggy Sanatine, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|December 25, 2025
Transgene-Induced Cardiotoxicity In High-Dose AAV Gene TransferAriane Biquand, Evelyne Gicquel, Jerome Poupiot, et al.
Pageof 1