Bjeloš, M.;                     Ćurić, A.;                     Rak, B.;                     Bušić, M.;                     Kuzmanović Elabjer, B.    
        The First Homozygote Mutation c.499G>T (Asp167Tyr) in the RPE65 Gene Encoding Retinoid Isomerohydrolase Causing Retinal Dystrophy. Curr. Issues Mol. Biol. 2022, 44, 6397-6403.
    https://doi.org/10.3390/cimb44120436
    AMA Style
    
                                Bjeloš M,                                 Ćurić A,                                 Rak B,                                 Bušić M,                                 Kuzmanović Elabjer B.        
                The First Homozygote Mutation c.499G>T (Asp167Tyr) in the RPE65 Gene Encoding Retinoid Isomerohydrolase Causing Retinal Dystrophy. Current Issues in Molecular Biology. 2022; 44(12):6397-6403.
        https://doi.org/10.3390/cimb44120436
    
    Chicago/Turabian Style
    
                                Bjeloš, Mirjana,                                 Ana Ćurić,                                 Benedict Rak,                                 Mladen Bušić,                                 and Biljana Kuzmanović Elabjer.        
                2022. "The First Homozygote Mutation c.499G>T (Asp167Tyr) in the RPE65 Gene Encoding Retinoid Isomerohydrolase Causing Retinal Dystrophy" Current Issues in Molecular Biology 44, no. 12: 6397-6403.
        https://doi.org/10.3390/cimb44120436
    
    APA Style
    
                                Bjeloš, M.,                                 Ćurić, A.,                                 Rak, B.,                                 Bušić, M.,                                 & Kuzmanović Elabjer, B.        
        
        (2022). The First Homozygote Mutation c.499G>T (Asp167Tyr) in the RPE65 Gene Encoding Retinoid Isomerohydrolase Causing Retinal Dystrophy. Current Issues in Molecular Biology, 44(12), 6397-6403.
        https://doi.org/10.3390/cimb44120436