Keratitis-ichthyosis-deafness syndrome with heterozygous p.D50N in the GJB2 gene in two Serbian adult patients
By:
Authors
T Kalezić
School of Medicine, University of Belgrade; Clinic for Eye Disease, University Clinical Centre of Serbia, Belgrade, Serbia
I Vuković
School of Medicine, University of Belgrade; Clinic for Gynecology and Obstetrics, University Clinical Centre of Serbia, Belgrade, Serbia
M Stojković
School of Medicine, University of Belgrade; Clinic for Eye Disease, University Clinical Centre of Serbia, Belgrade, Serbia
S Stanojlović
School of Medicine, University of Belgrade; Clinic for Eye Disease, University Clinical Centre of Serbia, Belgrade, Serbia
J Karanović
University of Belgrade, Faculty of Biology, Center for Human Molecular Genetics, Belgrade, Serbia
G Brajušković
University of Belgrade, Faculty of Biology, Center for Human Molecular Genetics, Belgrade, Serbia
D Savić-Pavićević
University of Belgrade, Faculty of Biology, Center for Human Molecular Genetics, Belgrade, Serbia
DOI: https://doi.org/10.2478/bjmg-2022-0014 | Journal eISSN: 2199-5761
Language: English
Page range: 79 - 84
Published on: Mar 1, 2023
Published by: Macedonian Academy of Sciences and Arts
In partnership with: Paradigm Publishing Services
Publication frequency: 2 issues per year
Keywords:
Related subjects:
© 2023 T Kalezić, I Vuković, M Stojković, S Stanojlović, J Karanović, G Brajušković, D Savić-Pavićević, published by Macedonian Academy of Sciences and Arts
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.