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CACT deficiency is a rare autosomal recessive disorder caused by SLC25A20 deficiency ( CACT, CPT2 , and LCAD , partially explaining the accumulation of ACs in children with abnormal liver function caused by VPA

WNT2 Locus Is Involved in Genetic Susceptibility of Peyronies Disease

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Under oxidative or inflammatory stress, TFAM is released into the cytoplasm along with mtDNA, where it interacts with the autophagy-associated protein LC3 to mediate the lysosomal clearance of both mtDNA and TFAM

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Consumption of meat, traditional and modern processed meat and colorectal cancer risk among the moroccan population: a large-scale case-control study