Janßen, S.; Erbe, L.S.; Kneifel, M.; Vorgerd, M.; Döring, K.; Lubieniecki, K.P.; Lubieniecka, J.M.; Gerding, W.M.; Casadei, N.; Güttsches, A.-K.;
et al. Compound Heterozygous RYR1 Variants in a Patient with Severe Congenital Myopathy: Case Report and Comparison with Additional Cases of Recessive RYR1-Related Myopathy. Int. J. Mol. Sci. 2024, 25, 10867.
https://doi.org/10.3390/ijms251910867
AMA Style
Janßen S, Erbe LS, Kneifel M, Vorgerd M, Döring K, Lubieniecki KP, Lubieniecka JM, Gerding WM, Casadei N, Güttsches A-K,
et al. Compound Heterozygous RYR1 Variants in a Patient with Severe Congenital Myopathy: Case Report and Comparison with Additional Cases of Recessive RYR1-Related Myopathy. International Journal of Molecular Sciences. 2024; 25(19):10867.
https://doi.org/10.3390/ijms251910867
Chicago/Turabian Style
Janßen, Sören, Leoni S. Erbe, Moritz Kneifel, Matthias Vorgerd, Kristina Döring, Krzysztof P. Lubieniecki, Joanna M. Lubieniecka, Wanda M. Gerding, Nicolas Casadei, Anne-Katrin Güttsches,
and et al. 2024. "Compound Heterozygous RYR1 Variants in a Patient with Severe Congenital Myopathy: Case Report and Comparison with Additional Cases of Recessive RYR1-Related Myopathy" International Journal of Molecular Sciences 25, no. 19: 10867.
https://doi.org/10.3390/ijms251910867
APA Style
Janßen, S., Erbe, L. S., Kneifel, M., Vorgerd, M., Döring, K., Lubieniecki, K. P., Lubieniecka, J. M., Gerding, W. M., Casadei, N., Güttsches, A.-K., Heyer, C., Lücke, T., Nguyen, H. H. P., Köhler, C., & Hoffjan, S.
(2024). Compound Heterozygous RYR1 Variants in a Patient with Severe Congenital Myopathy: Case Report and Comparison with Additional Cases of Recessive RYR1-Related Myopathy. International Journal of Molecular Sciences, 25(19), 10867.
https://doi.org/10.3390/ijms251910867
