Keratitis-ichthyosis-deafness syndrome with heterozygous p.D50N in the GJB2 gene in two Serbian adult patients
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01 mar 2023
INFORMAZIONI SU QUESTO ARTICOLO
Categoria dell'articolo: Case report
Pubblicato online: 01 mar 2023
Pagine: 79 - 84
DOI: https://doi.org/10.2478/bjmg-2022-0014
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© 2022 Kalezić T., Vuković I., Stojković M., Stanojlović S., Karanović J., Brajušković G., Savić-Pavićević D., published by Sciendo
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.
Kalezić, T
School of Medicine, University of Belgrade; Clinic for Eye Disease, University Clinical Centre of SerbiaBelgrade, Serbia
Vuković, I
School of Medicine, University of Belgrade; Clinic for Gynecology and Obstetrics, University Clinical Centre of SerbiaBelgrade, Serbia
Stojković, M
School of Medicine, University of Belgrade; Clinic for Eye Disease, University Clinical Centre of SerbiaBelgrade, Serbia
Stanojlović, S
School of Medicine, University of Belgrade; Clinic for Eye Disease, University Clinical Centre of SerbiaBelgrade, Serbia
Karanović, J
University of Belgrade, Faculty of Biology, Center for Human Molecular GeneticsBelgrade, Serbia
Brajušković, G
University of Belgrade, Faculty of Biology, Center for Human Molecular GeneticsBelgrade, Serbia
Savić-Pavićević, D
University of Belgrade, Faculty of Biology, Center for Human Molecular GeneticsBelgrade, Serbia