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Keratitis-ichthyosis-deafness syndrome with heterozygous p.D50N in the GJB2 gene in two Serbian adult patients

T Kalezić

T Kalezić

School of Medicine, University of Belgrade; Clinic for Eye Disease, University Clinical Centre of SerbiaBelgrade, Serbia
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Kalezić, T
, 
I Vuković

I Vuković

School of Medicine, University of Belgrade; Clinic for Gynecology and Obstetrics, University Clinical Centre of SerbiaBelgrade, Serbia
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Vuković, I
, 
M Stojković

M Stojković

School of Medicine, University of Belgrade; Clinic for Eye Disease, University Clinical Centre of SerbiaBelgrade, Serbia
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Stojković, M
, 
S Stanojlović

S Stanojlović

School of Medicine, University of Belgrade; Clinic for Eye Disease, University Clinical Centre of SerbiaBelgrade, Serbia
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Stanojlović, S
, 
J Karanović

J Karanović

University of Belgrade, Faculty of Biology, Center for Human Molecular GeneticsBelgrade, Serbia
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Karanović, J
, 
G Brajušković

G Brajušković

University of Belgrade, Faculty of Biology, Center for Human Molecular GeneticsBelgrade, Serbia
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Brajušković, G
 and 
D Savić-Pavićević

D Savić-Pavićević

University of Belgrade, Faculty of Biology, Center for Human Molecular GeneticsBelgrade, Serbia
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Savić-Pavićević, D
  
Mar 01, 2023
Keratitis-ichthyosis-deafness syndrome with heterozygous p.D50N in the GJB2 gene in two Serbian adult patients's Cover Image
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Article Category: Case report
Published Online: Mar 01, 2023
Page range: 79 - 84
DOI: https://doi.org/10.2478/bjmg-2022-0014
Keywords
© 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.
Language:
English
Publication timeframe:
2 times per year
Journal Subjects:
Medicine, Basic Medical Science, Basic Medical Science, other
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