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Description
The total read counts were verified using the log output files generated by STAR

Mitochondrial HMG-CoA synthase deficiency is a rare autosomal disorder

Rats with none or one mutant allele are of the lean phenotype (L-ZSF1) and do not develop HFpEF

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Ooi EMM, Barrett PHR, Chan DC, Watts GF

, Backhed F., Turnbaugh P., Lozupone C
