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Mutations in CPT1 can cause carnitine palmitoyltransferase I (CPT I) deficiency, which is an autosomal recessive genetic condition (need two copies of the mutation)

Pyridoxine (Vitamin B6): Crucial for metabolizing fats, carbohydrates, and proteins, speeding up your metabolism to burn calories and lose weight quicker while aiding in nutrient extraction from food

Notably, a single mtDNA mutation has minimal impact on the physiological phenotype, and it is only when the number of mutant mtDNAs exceeds a threshold that cellular function is compromised