Article Versions Notes

Erbe LS, Hoffjan S, Janßen S, Kneifel M, Krause K, Gerding WM, Döring K, Güttsches A-K, Roos A, Buena Atienza E, et al. Exome Sequencing and Optical Genome Mapping in Molecularly Unsolved Cases of Duchenne Muscular Dystrophy: Identification of a Causative X-Chromosomal Inversion Disrupting the DMD Gene. International Journal of Molecular Sciences. 2023; 24(19):14716. https://doi.org/10.3390/ijms241914716

Erbe, Leoni S., Sabine Hoffjan, Sören Janßen, Moritz Kneifel, Karsten Krause, Wanda M. Gerding, Kristina Döring, Anne-Katrin Güttsches, Andreas Roos, Elena Buena Atienza, and et al. 2023. "Exome Sequencing and Optical Genome Mapping in Molecularly Unsolved Cases of Duchenne Muscular Dystrophy: Identification of a Causative X-Chromosomal Inversion Disrupting the DMD Gene" International Journal of Molecular Sciences 24, no. 19: 14716. https://doi.org/10.3390/ijms241914716

Erbe, L. S., Hoffjan, S., Janßen, S., Kneifel, M., Krause, K., Gerding, W. M., Döring, K., Güttsches, A.-K., Roos, A., Buena Atienza, E., Gross, C., Lücke, T., Nguyen, H. H. P., Vorgerd, M., & Köhler, C. (2023). Exome Sequencing and Optical Genome Mapping in Molecularly Unsolved Cases of Duchenne Muscular Dystrophy: Identification of a Causative X-Chromosomal Inversion Disrupting the DMD Gene. International Journal of Molecular Sciences, 24(19), 14716. https://doi.org/10.3390/ijms241914716