Coenzyme Q10 supplementation therapy for 2 children with proteinuria renal disease and ADCK4 mutation
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
General Medicine
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3. Leigh syndrome with nephropathy and CoQ10 deficiency due to decaprenyl diphosphate synthase subunit 2 (PDSS2) mutations;López;Am J Hum Genet,2006
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