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Mutations in the gene encoding OCTN2, SLC22A5 , can impair fatty acid metabolism and lead to systemic primary carnitine deficiency (SPCD, OMIM 212140) 8 , an autosomal recessive disorder whose clinical manifestations include cardiomyopathy, hypoglycemia, chronic muscle weakness and liver dysfunction 9

A., Flory, J., Rowan, C

doi: 10.3389/fphar.2021.780924 42 JiaJ.DouP.GaoM.KongX.LiC.LiuZ.et al

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Electrochemical methods, in comparison to traditional chromatographic techniques, exhibit characteristics of high sensitivity and low cost, thus conferring significant advantages in the field of biomedicine

Human immunodeficiency virus (HIV) and hepatitis C infection are well known to be associated with small fiber neuropathy, so relevant risk factors (eg, blood transfusions, sexual history, intravenous drug use) should be asked about