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, High-dose coenzyme Q10 therapy versus placebo in patients with post COVID-19 condition: A randomized, phase 2, crossover trial
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While mutations in either the PCCA or PCCB gene cause propionic acidemia (MIM# 606054), isolated methylmalonic acidemia is caused either by a genetic defect in the MUT enzyme itself (MIM# 251000, MMA mut type), or in one of the proteins (MMAA, MMAB, MMADHC) involved in the synthesis of its active cofactor, adenosylobalamin (MMA cblA type, MIM# 251100
