Library

Duan, D., Goemans, N., Takeda, S. et al. Duchenne muscular dystrophy. Nat Rev Dis Primers 7, 13 (2021). https://doi.org/10.1038/s41572-021-00248-3 Abstract Duchenne muscular dystrophy is…

Zimowski JG, Purzycka J, Pawelec M, Ozdarska K, Zaremba J. Small mutations in Duchenne/Becker muscular dystrophy in 164 unrelated Polish…

Selvatici R, Rossi R, Fortunato F, et al. Ethnicity-related DMD Genotype Landscapes in European and Non-European Countries. Neurol Genet 2021;7:e536…

Uechi L, Jalali M, Wilbur JD, et al. Complex genetic dependencies among growth and neurological phenotypes in healthy children: Towards…

Lim KRQ, Nguyen Q, Yokota T. Genotype-Phenotype Correlations in Duchenne and Becker Muscular Dystrophy Patients from the Canadian Neuromuscular Disease…

de Feraudy Y, Yaou RB, Wahbi K, et al. Very low residual dystrophin quantity is associated with milder dystrophinopathy. Annals…

Keegan NP. Pseudoexons of the DMD Gene. Journal of neuromuscular diseases 2020;7:77-95   Abstract The DMD gene is the largest…

Traverso M, Assereto S, Baratto S, et al. Clinical and molecular consequences of exon 78 deletion in DMD gene. J…

Haber G, Conway KM, Paramsothy P, et al. Association of genetic mutations and loss of ambulation in childhood-onset dystrophinopathy. Muscle…

Sato T, Wakita M, Matsushima M, Sato T. A novel deletion of the dystrophin gene in a patient without muscle-related…