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

A Paripović

A Paripović

  • Department of Nephrology, Mother and Child Health Care Institute of Serbia “Dr Vukan Čupić”Belgrade, Serbia
  • University of Belgrade, Faculty of Medicine
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Paripović, A
, 
A Maver

A Maver

Clinical Institute of Genomic Medicine, University Medical Centre LjubljanaLjubljana, Slovenia
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Maver, A
, 
N Stajić

N Stajić

  • Department of Nephrology, Mother and Child Health Care Institute of Serbia “Dr Vukan Čupić”Belgrade, Serbia
  • University of Belgrade, Faculty of Medicine
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Stajić, N
, 
J Putnik

J Putnik

  • Department of Nephrology, Mother and Child Health Care Institute of Serbia “Dr Vukan Čupić”Belgrade, Serbia
  • University of Belgrade, Faculty of Medicine
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Putnik, J
, 
S Ostojić

S Ostojić

  • Department of Neurology, Mother and Child Health Care Institute of Serbia “Dr Vukan Čupić”Belgrade, Serbia
  • University of Belgrade, Faculty of Medicine
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Ostojić, S
, 
B Alimpić

B Alimpić

Day Care Hospital, Mother and Child Health Care Institute of Serbia “Dr Vukan Čupić”Belgrade, Serbia
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Alimpić, B
, 
N Ilić

N Ilić

Clinical Genetics Outpatient Clinic, Mother and Child Health Care Institute of Serbia “Dr Vukan Čupić”Belgrade, Serbia
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Ilić, N
 and 
A Sarajlija

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
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Sarajlija, A
  
Mar 12, 2024
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Article Category: Case Report
Published Online: Mar 12, 2024
Page range: 59 - 64
DOI: https://doi.org/10.2478/bjmg-2023-0016
Keywords
© 2023 A Paripović et al., 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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