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[DOI] [PubMed] [Google Scholar] [81].Nakamura HMH, Yodoi J

& Hofmann, A

An alternative strategy of starting the diagnostic investigation with mRNA sequencing has also been recommended, particularly because of the delay in diagnosis that can occur when glutathione synthetase deficiency results from a splice site mutation (02)

It could be shown that SjTrx1i could reduce insulin with both electron donors, but SjTRP14 could not (Fig 5C-5D), indicating that SjTRP14 exhibited no insulin-reducing activity, either with DTT or when coupled with the SjTGR enzymatic reducing system