Mutant mitochondrial thymidine kinase in mitochondrial DNA depletion myopathyAnn Saada, Orly Elpeleg, Avraham Shaag et al.|Nature Genetics|2001Cited by 618
Nuclear envelope dystrophies show a transcriptional fingerprint suggesting disruption of Rb–MyoD pathways in muscle regenerationMarina Bakay, Eric P. Hoffman, Zuyi Wang et al.|Brain|2006Cited by 329
Mutations in KLHL40 Are a Frequent Cause of Severe Autosomal-Recessive Nemaline MyopathyGianina Ravenscroft, Alan H. Beggs, Kyle S. Yau et al.|The American Journal of Human Genetics|2013Cited by 224
Life or death by NFκB, Losartan promotes survival in dy2J/dy2J mouse of MDC1AMoran Elbaz, Yoram Nevo|Cell Death and Disease|2015Cited by 18
Long‐Term Evaluation of Givinostat in Duchenne Muscular Dystrophy, and Natural History ComparisonsCraig M. McDonald, Michela Guglieri, Dragana Vučinić et al.|Annals of Clinical and Translational Neurology|2025Cited by 12