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The genetics of asthma: are the glutathione S-transferases serious players
Dieser genetisch bedingte primre L-Carnitin Mangel wurde erstmals 1973 festgestellt und steigerte das mediale Interesse an L-Carnitin
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Site-directed mutagenesis and inhibition assays revealed that Phe-9 is potentially an important residue for the binding of the inhibitor S-hexyl glutathione (GTX) [77]
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