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The effect of homozygous deletion of the BBOX1 and Fibin genes on carnitine level and acyl carnitine profile

Loss of function of CAV1 cause Berardinelli-Seip congenital lipodystrophy and congenital generalized lipodystrophy type 3 (OMIM #612526), characterized by marked paucity of adipose tissue, extreme insulin resistance, hypertriglyceridemia, hepatic steatosis, and early onset of diabetes [43]

Gesuete, V., Ragni, L., and Picchio, F

We repeated the analysis by sex and tested for differences between the estimates using a heterogeneity test [40]

c p-value based on analysis of covariance (ANCOVA) (comparison of data between the groups post-intervention, adjusted for baseline values, changes in physical activity, energy intake, and BMI)