Maggi, J.; Feil, S.; Gloggnitzer, J.; Maggi, K.; Bachmann-Gagescu, R.; Gerth-Kahlert, C.; Koller, S.; Berger, W.
Nanopore Deep Sequencing as a Tool to Characterize and Quantify Aberrant Splicing Caused by Variants in Inherited Retinal Dystrophy Genes. Int. J. Mol. Sci. 2024, 25, 9569.
https://doi.org/10.3390/ijms25179569
AMA Style
Maggi J, Feil S, Gloggnitzer J, Maggi K, Bachmann-Gagescu R, Gerth-Kahlert C, Koller S, Berger W.
Nanopore Deep Sequencing as a Tool to Characterize and Quantify Aberrant Splicing Caused by Variants in Inherited Retinal Dystrophy Genes. International Journal of Molecular Sciences. 2024; 25(17):9569.
https://doi.org/10.3390/ijms25179569
Chicago/Turabian Style
Maggi, Jordi, Silke Feil, Jiradet Gloggnitzer, Kevin Maggi, Ruxandra Bachmann-Gagescu, Christina Gerth-Kahlert, Samuel Koller, and Wolfgang Berger.
2024. "Nanopore Deep Sequencing as a Tool to Characterize and Quantify Aberrant Splicing Caused by Variants in Inherited Retinal Dystrophy Genes" International Journal of Molecular Sciences 25, no. 17: 9569.
https://doi.org/10.3390/ijms25179569
APA Style
Maggi, J., Feil, S., Gloggnitzer, J., Maggi, K., Bachmann-Gagescu, R., Gerth-Kahlert, C., Koller, S., & Berger, W.
(2024). Nanopore Deep Sequencing as a Tool to Characterize and Quantify Aberrant Splicing Caused by Variants in Inherited Retinal Dystrophy Genes. International Journal of Molecular Sciences, 25(17), 9569.
https://doi.org/10.3390/ijms25179569