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CoenzymeQ10 therapy in two sisters with CoQ6 mutations with long-term follow-up

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References

  1. Stańczyk M, Bałasz-Chmielewska I, Lipska-Ziętkiewicz B, Tkaczyk M (2018) CoQ10-related sustained remission of proteinuria in a child with COQ6 glomerulopathy-a case report. Pediatr Nephrol 33:2383–2387

    Article  PubMed  PubMed Central  Google Scholar 

  2. Heeringa SF, Chernin G, Chaki M, Zhou W, Sloan AJ, Ji Z, Xie LX, Salviati L, Hurd TW, Vega-Warner V, Killen PD, Raphael Y, Ashraf S, Ovunc B, Schoeb DS, McLaughlin HM, Airik R, Vlangos CN, Gbadegesin R, Hinkes B, Saisawat P, Trevisson E, Doimo M, Casarin A, Pertegato V, Giorgi G, Prokisch H, Rötig A, Nürnberg G, Becker C, Wang S, Ozaltin F, Topaloglu R, Bakkaloglu A, Bakkaloglu SA, Müller D, Beissert A, Mir S, Berdeli A, Varpizen S, Zenker M, Matejas V, Santos-Ocaña C, Navas P, Kusakabe T, Kispert A, Akman S, Soliman NA, Krick S, Mundel P, Reiser J, Nürnberg P, Clarke CF, Wiggins RC, Faul C, Hildebrandt F (2011) COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness. J Clin Invest 121:2013–2024

    Article  CAS  PubMed  PubMed Central  Google Scholar 

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Correspondence to Mustafa Koyun.

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Koyun, M., Çomak, E. & Akman, S. CoenzymeQ10 therapy in two sisters with CoQ6 mutations with long-term follow-up. Pediatr Nephrol 34, 737–738 (2019). https://doi.org/10.1007/s00467-018-4150-9

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  • DOI: https://doi.org/10.1007/s00467-018-4150-9

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