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This would explain why Pdss2 kd/kd mutants mainly develop a renal phenotype, despite widespread CoQ 9 deficiency (30, 124)
[DOI] [PMC free article] [PubMed] [Google Scholar] 74.Zhang Z., Yu L., Li S., Liu J
DOI: 10.1111/nmo.14181
doi: 10.18388/abp.2007_3264, 146
