Erbe, L.S.; Hoffjan, S.; Janßen, S.; Kneifel, M.; Krause, K.; Gerding, W.M.; 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. Int. J. Mol. Sci. 2023, 24, 14716.
https://doi.org/10.3390/ijms241914716
AMA Style
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
Chicago/Turabian Style
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
APA Style
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