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CACT deficiency is a rare autosomal recessive disorder caused by SLC25A20 deficiency (Rubio-Gozalbo et al., 2004)

An experienced injector or nurse will guide you on dosing, frequency, and expectations

Wong WT, Kam W, Cunningham D, Harrington M, Hammel K, Meyerle CB, Cukras C, Chew EY, Sadda SR, Ferris FL

The LPS-TLR4-JNK/NF-B axis disrupts mitochondrial membrane potential and cristae architecture while downregulating Parkin expression, thereby blocking PINK1/Parkin-mediated mitochondrial autophagy

Morrow PK, D'Souza S, Wood T, Gowda V, Lee N, Zhang ML, et al

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