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Low-Frequency and Rare Exome Chip Variants Associate with Fasting Glucose and Type 2 Diabetes Susceptibility. Nature Communications, vol

Introduction Methylmalonic Acidemia (MMA) is an autosomal recessively inherited organic acid disorder due to deficient activity of mitochondrial B12-dependent methylmalonyl-CoA mutase, an enzyme which limits the conversion of methylmalonyl-CoA to succinyl-CoA

LDN has two downsides: It requires a doctors prescription and must be purchased from a compounding pharmacy

Protein concentrations were measured by the bicinchoninic acid method (Pierce Biotechnology, Inc., Rockford, IL, USA)

Furthermore, it is essential to include a more diverse sample in future research, accounting for factors like age, gender, and training status, to ensure that the results are more generalized

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