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