Have a personal or library account? Click to login
Expanding the Phenotypic Spectrum: Chronic Kidney Disease in a Patient with Combined Oxidative Phosphorylation Defect 21 Cover

Expanding the Phenotypic Spectrum: Chronic Kidney Disease in a Patient with Combined Oxidative Phosphorylation Defect 21

Open Access
|Mar 2024

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

adrijans2004@yahoo.com

Clinical Genetics Outpatient Clinic, Mother and Child Health Care Institute of Serbia “Dr Vukan Čupić”, Belgrade, Serbia
University of Belgrade, Faculty of Medicine
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

© 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.