Expanding the Phenotypic Spectrum: Chronic Kidney Disease in a Patient with Combined Oxidative Phosphorylation Defect 21
By: A Paripović, A Maver, N Stajić, J Putnik, S Ostojić, B Alimpić, N Ilić and A Sarajlija
Authors
A Paripović
Department of Nephrology, Mother and Child Health Care Institute of Serbia “Dr Vukan Čupić”, Belgrade, Serbia
University of Belgrade, Faculty of Medicine
A Maver
Clinical Institute of Genomic Medicine, University Medical Centre Ljubljana, Ljubljana, Slovenia
N Stajić
Department of Nephrology, Mother and Child Health Care Institute of Serbia “Dr Vukan Čupić”, Belgrade, Serbia
University of Belgrade, Faculty of Medicine
J Putnik
Department of Nephrology, Mother and Child Health Care Institute of Serbia “Dr Vukan Čupić”, Belgrade, Serbia
University of Belgrade, Faculty of Medicine
S Ostojić
Department of Neurology, Mother and Child Health Care Institute of Serbia “Dr Vukan Čupić”, Belgrade, Serbia
University of Belgrade, Faculty of Medicine
B Alimpić
Day Care Hospital, Mother and Child Health Care Institute of Serbia “Dr Vukan Čupić”, Belgrade, Serbia
N Ilić
Clinical Genetics Outpatient Clinic, Mother and Child Health Care Institute of Serbia “Dr Vukan Čupić”, Belgrade, Serbia
A Sarajlija
Clinical Genetics Outpatient Clinic, Mother and Child Health Care Institute of Serbia “Dr Vukan Čupić”, Belgrade, Serbia
University of Belgrade, Faculty of Medicine
DOI: https://doi.org/10.2478/bjmg-2023-0016 | Journal eISSN: 2199-5761
Language: English
Page range: 59 - 64
Published on: Mar 12, 2024
Published by: Macedonian Academy of Sciences and Arts
In partnership with: Paradigm Publishing Services
Publication frequency: 2 issues per year
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© 2024 A Paripović, A Maver, N Stajić, J Putnik, S Ostojić, B Alimpić, N Ilić, A Sarajlija, published by Macedonian Academy of Sciences and Arts
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.