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