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

被引：0
作者：
Mustafa Koyun
Elif Çomak
Sema Akman
机构：
[1] Akdeniz University,School of Medicine, Department of Pediatrics, Division of Pediatric Nephrology
来源：
Pediatric Nephrology | 2019年 / 34卷
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页码：737 / 738
页数：1
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  • [1] Stańczyk M(2018)CoQ10-related sustained remission of proteinuria in a child with COQ6 glomerulopathy-a case report Pediatr Nephrol 33 2383-2387
  • [2] Bałasz-Chmielewska I(2011)COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness J Clin Invest 121 2013-2024
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