Kivrak Pfiffner, F.; Koller, S.; Ménétrey, A.; Graf, U.; Bähr, L.; Maspoli, A.; Hackenberg, A.; Kottke, R.; Gerth-Kahlert, C.; Berger, W.
Homozygosity for a Novel DOCK7 Variant Due to Segmental Uniparental Isodisomy of Chromosome 1 Associated with Early Infantile Epileptic Encephalopathy (EIEE) and Cortical Visual Impairment. Int. J. Mol. Sci. 2022, 23, 7382.
https://doi.org/10.3390/ijms23137382
AMA Style
Kivrak Pfiffner F, Koller S, Ménétrey A, Graf U, Bähr L, Maspoli A, Hackenberg A, Kottke R, Gerth-Kahlert C, Berger W.
Homozygosity for a Novel DOCK7 Variant Due to Segmental Uniparental Isodisomy of Chromosome 1 Associated with Early Infantile Epileptic Encephalopathy (EIEE) and Cortical Visual Impairment. International Journal of Molecular Sciences. 2022; 23(13):7382.
https://doi.org/10.3390/ijms23137382
Chicago/Turabian Style
Kivrak Pfiffner, Fatma, Samuel Koller, Anika Ménétrey, Urs Graf, Luzy Bähr, Alessandro Maspoli, Annette Hackenberg, Raimund Kottke, Christina Gerth-Kahlert, and Wolfgang Berger.
2022. "Homozygosity for a Novel DOCK7 Variant Due to Segmental Uniparental Isodisomy of Chromosome 1 Associated with Early Infantile Epileptic Encephalopathy (EIEE) and Cortical Visual Impairment" International Journal of Molecular Sciences 23, no. 13: 7382.
https://doi.org/10.3390/ijms23137382
APA Style
Kivrak Pfiffner, F., Koller, S., Ménétrey, A., Graf, U., Bähr, L., Maspoli, A., Hackenberg, A., Kottke, R., Gerth-Kahlert, C., & Berger, W.
(2022). Homozygosity for a Novel DOCK7 Variant Due to Segmental Uniparental Isodisomy of Chromosome 1 Associated with Early Infantile Epileptic Encephalopathy (EIEE) and Cortical Visual Impairment. International Journal of Molecular Sciences, 23(13), 7382.
https://doi.org/10.3390/ijms23137382