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coenzyme q10 deficiency
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COQ2
Isolation and functional expression of human COQ2, a gene encoding a polyprenyl transferase involved in the synthesis of CoQ
PDSS1
Quinone-responsive multiple respiratory-chain dysfunction due to widespread coenzyme Q10 deficiency
PDSS2
Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library.
Candidate gene/loci studies in cleft lip/palate and dental anomalies finds novel susceptibility genes for clefts.
COQ9
A Mouse for All Reasons
COQ6
COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness
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