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10.1016/j.ophtha.2005.04.018 Ophthalmology 46 Diabetes Control and Complications Trial Research GroupNathanD

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Disorders of organic acid metabolism Methylmalonic acidemia Methylmalonic acidemia (MMA) is an autosomal recessive disorder caused by a deficiency in methylmalonyl coenzyme A (CoA) mutase (MUT), which is encoded by the MUT gene

As a long-acting peptide analog, Cagrilintide represents a research subject in the broader field of peptide stability engineering specifically the use of fatty acid acylation strategies to extend peptide half-life and enzymatic resistance compared to native peptide sequences