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Chi J, Chen Y, Li C, Liu S, Che K, Kong Z, et al

Rare mutations in SLC22A5 can cause hypoglycemia and liver problems from infancy, and this is one of the genetic conditions that is usually screened for at birth

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By influencing NNMT-associated pathways, it serves as a valuable tool in in vitro studies examining metabolic regulation, mitochondrial function, and potential applications in obesity and age-related research contexts

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